Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,116 results
Food & BeverageFranceRappelConso

disney - fleurs de douche simba -gencod 3666085407553 -tous les lots

disney
RappelConsovolontaire (san...

disney - fleurs de douche simba -gencod 3666085407553 -tous les lots

présence de phtalates dans le badge décoratif amovible associé à la fleur de douche - personnage simba. ces composés ont des effets négatifs sur la santé.

Mar 18, 2026disney
Food & BeverageFranceRappelConso

travel folding electeic kettle bouilloire électrique

Unknown Firm
RappelConsoGeneral Alert

travel folding electeic kettle bouilloire électrique

le produit n'a pas une résistance mécanique suffisante et pourrait donc facilement se casser en cas d'impact ou de chute du produit. de plus, les connecteurs des fils alimentant l'interrupteur bimétallique et l'élément chauffant ne sont pas correctement sertis et pourraient se détacher avec le temps. le produit a également des distances de dégagement insuffisantes. tout cela pourrait rendre les pièces sous tension accessibles à l'utilisateur, qui pourrait recevoir un choc électrique. de plus, la prise électrique n'est pas conforme, ce qui pourrait entraîner une connexion lâche et une surchauffe du produit.

Mar 18, 2026
Medical DeviceUSFDA Devices

GEM Premier 5000 PAK; Part No. 00055415004.

Instrumentation Laboratory
FDA DevicesClass II

GEM Premier 5000 PAK; Part No. 00055415004.

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

Mar 18, 2026Instrumentation Laboratory
Medical DeviceUSFDA Devices

CLARITY II Laser System; Model No. 1110200210.

Lutronic Corporation
FDA DevicesClass II

CLARITY II Laser System; Model No. 1110200210.

Reports of devices sparking/popping and potentially burning patients.

Mar 18, 2026Lutronic Corporation
Food & BeverageUSFDA Food

VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Vegetable oil***" Contains: Wheat, Soy. UPC 8 10037 81061 5 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138

Palmetto Gourmet Foods Inc.
FDA FoodClass II

VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***) Vegetable oil***" Contains: Wheat, Soy. UPC 8 10037 81061 5 Produced by PALMETTO GOURMET FOODS, INC SALUDA, SC 29138

Product contains undeclared Yellow #5

Mar 18, 2026Palmetto Gourmet Foods Inc.
Medical DeviceUSFDA Devices

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

Waldemar Link GmbH & Co. KG (Mfg Site)
FDA DevicesClass II

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Mar 18, 2026Waldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceUSFDA Devices

Endo-Model Replacement Plateau; Item Number: 15-0027/16;

Waldemar Link GmbH & Co. KG (Mfg Site)
FDA DevicesClass II

Endo-Model Replacement Plateau; Item Number: 15-0027/16;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Mar 18, 2026Waldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceUSFDA Devices

GEM Premier 5000; Part No. 00055430011.

Instrumentation Laboratory
FDA DevicesClass II

GEM Premier 5000; Part No. 00055430011.

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

Mar 18, 2026Instrumentation Laboratory
Medical DeviceUSFDA Devices

Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.

Medartis AG
FDA DevicesClass II

Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.

Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.

Mar 18, 2026Medartis AG
Medical DeviceUSFDA Devices

Endo-Model Replacement Plateau; Item Number: 15-2836/11;

Waldemar Link GmbH & Co. KG (Mfg Site)
FDA DevicesClass II

Endo-Model Replacement Plateau; Item Number: 15-2836/11;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Mar 18, 2026Waldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceUSFDA Devices

Endo-Model Replacement Plateau; Item Number: 15-8521/11;

Waldemar Link GmbH & Co. KG (Mfg Site)
FDA DevicesClass II

Endo-Model Replacement Plateau; Item Number: 15-8521/11;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

Mar 18, 2026Waldemar Link GmbH & Co. KG (Mfg Site)
Food & BeverageUSFDA Food

Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were sold frozen in bulk packaging to grocery retailers' in-store bakeries. They are intended to be baked by the retailer before consumer sale. Frozen raw pies were not sold to consumers at retail stores. Product is labeled with BAKING INSTRUCTIONS: Preheat convection oven to 340 degrees Fahrenheit. Bake pies for 70-80 minutes. Ovens will vary. Adjust time and temperature accordingly to ensure center of pie reaches 210F.

Willamette Valley Pie Company, LLC
FDA FoodClass II

Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were sold frozen in bulk packaging to grocery retailers' in-store bakeries. They are intended to be baked by the retailer before consumer sale. Frozen raw pies were not sold to consumers at retail stores. Product is labeled with BAKING INSTRUCTIONS: Preheat convection oven to 340 degrees Fahrenheit. Bake pies for 70-80 minutes. Ovens will vary. Adjust time and temperature accordingly to ensure center of pie reaches 210F.

Potential contamination with listeria monocytogenes.

Mar 18, 2026Willamette Valley Pie Company, LLC
Food & BeverageUSFDA Food

Lowes Foods sour cream and onion flavored potato chips, 8oz. bag, UPC 7 41643 05576 6, 9 retail units per case

Uncle Ray's LLC
FDA FoodClass II

Lowes Foods sour cream and onion flavored potato chips, 8oz. bag, UPC 7 41643 05576 6, 9 retail units per case

Inaccurate nutritional data in Nutrition Facts including but not limited to, understated sodium content. Undeclared ingredients including but not limited to, monosodium glutamate.

Mar 18, 2026Uncle Ray's LLC
Medical DeviceUSFDA Devices

Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2

Penner Patient Care, Inc.
FDA DevicesClass III

Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2

The device does not bear a unique device identifier.

Mar 18, 2026Penner Patient Care, Inc.
Medical DeviceUSFDA Devices

Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobile Shower Commode Chair, Catalog Number Z333 UDI-DI code: (01)00628758003335 Raz-AT600 (Bariatric Tilt) Mobile Shower Commode Chair, Catalog Number Z360 UDI-DI code: (01)00628758003601 Raz-SP (Self Propel) Mobile Shower Commode Chair, Catalog Number Z200 UDI-DI code: (01)00628758001003 Raz-AP (Attendant Propel) Mobile Shower Commode Chair, Catalog Number Z100 UDI-DI code: (01)00628758001003 The Raz Mobile Shower Commode Chair is intended to be used by people with mobility impairments, who may have difficulty in standing or keeping their balance while completing activities such as showering, toileting, or personal hygiene.

Raz Design Inc
FDA DevicesClass II

Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobile Shower Commode Chair, Catalog Number Z333 UDI-DI code: (01)00628758003335 Raz-AT600 (Bariatric Tilt) Mobile Shower Commode Chair, Catalog Number Z360 UDI-DI code: (01)00628758003601 Raz-SP (Self Propel) Mobile Shower Commode Chair, Catalog Number Z200 UDI-DI code: (01)00628758001003 Raz-AP (Attendant Propel) Mobile Shower Commode Chair, Catalog Number Z100 UDI-DI code: (01)00628758001003 The Raz Mobile Shower Commode Chair is intended to be used by people with mobility impairments, who may have difficulty in standing or keeping their balance while completing activities such as showering, toileting, or personal hygiene.

Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.

Mar 18, 2026Raz Design Inc
Medical DeviceUSFDA Devices

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.

Medartis AG
FDA DevicesClass II

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.

Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.

Mar 18, 2026Medartis AG
Food & BeverageUSFDA Food

Coco's Italian Market Heat-n-Eat Fettuccini Alfredo in homemade Alfredo Sauce, Net Wt. 19 oz. (510g), Keep Frozen, packaged in a microwaveable plastic container, UPC 0680334993607

Cocos Wholesale and Imports, LLC
FDA FoodClass II

Coco's Italian Market Heat-n-Eat Fettuccini Alfredo in homemade Alfredo Sauce, Net Wt. 19 oz. (510g), Keep Frozen, packaged in a microwaveable plastic container, UPC 0680334993607

Label lists semolina and durum flour as sub-ingredients of the pasta, but does not declare wheat

Mar 18, 2026Cocos Wholesale and Imports, LLC
Food & BeverageUSFDA Food

House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub

House Of Flavors, Inc.
FDA FoodClass I

House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub

Undeclared egg

Mar 18, 2026House Of Flavors, Inc.
PharmaceuticalUSFDA Drugs

Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1592-7

Zydus Pharmaceuticals (USA) Inc
FDA DrugsClass II

Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1592-7

Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.

Mar 18, 2026Zydus Pharmaceuticals (USA) Inc
Medical DeviceUSFDA Devices

GEM Premier 5000; Model No. 00055430010.

Instrumentation Laboratory
FDA DevicesClass II

GEM Premier 5000; Model No. 00055430010.

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

Mar 18, 2026Instrumentation Laboratory
Medical DeviceUSFDA Devices

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

Exactech, Inc.
FDA DevicesClass II

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

Impactor handle may be missing cross-pin

Mar 18, 2026Exactech, Inc.
Medical DeviceUSFDA Devices

GEM Premier 5000 PAK, Part No. 00055360004.

Instrumentation Laboratory
FDA DevicesClass II

GEM Premier 5000 PAK, Part No. 00055360004.

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

Mar 18, 2026Instrumentation Laboratory
Medical DeviceUSFDA Devices

Penner Pacific Bathing Spa, Model Numbers 360020-1EP

Penner Patient Care, Inc.
FDA DevicesClass III

Penner Pacific Bathing Spa, Model Numbers 360020-1EP

The device does not bear a unique device identifier.

Mar 18, 2026Penner Patient Care, Inc.
Food & BeverageUSFDA Food

Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVEM F.D. & C. YELLOW COLOR #5 & #6 (TARTRAZINE) ARTIFICIAL COLORS) Primary Packaging: CHINA NOODLE CO. STEAM NOODLE NET WEIGHT 10 LBS. (4536 grams) PERISHABLE KEEP REFRIGERATED INGREDIENTS: ENRICHED WHEAT FLOUR (BLEACHED WHEAT FLOUR, NIACIN, IRON, ASCORBIC ACID, THIAMIN MONONITRATE, RIBOFLAVIN), WATER, SALT, SOYBEAN OIL, SODIUM BI-CARBONATE, 1/1000 BENZOATE OF SODIUM, DUSTED WITH CORN STARCH, ADDED AS A PRESERVATIVE, F.D. & C. YELLOW COLOR #5 AND #6 (TARTRAZINE) (ARTIFICIAL COLORS). ALLERGY INFORMATION: WHEAT

CNC Noodle Corporation
FDA FoodClass II

Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVEM F.D. & C. YELLOW COLOR #5 & #6 (TARTRAZINE) ARTIFICIAL COLORS) Primary Packaging: CHINA NOODLE CO. STEAM NOODLE NET WEIGHT 10 LBS. (4536 grams) PERISHABLE KEEP REFRIGERATED INGREDIENTS: ENRICHED WHEAT FLOUR (BLEACHED WHEAT FLOUR, NIACIN, IRON, ASCORBIC ACID, THIAMIN MONONITRATE, RIBOFLAVIN), WATER, SALT, SOYBEAN OIL, SODIUM BI-CARBONATE, 1/1000 BENZOATE OF SODIUM, DUSTED WITH CORN STARCH, ADDED AS A PRESERVATIVE, F.D. & C. YELLOW COLOR #5 AND #6 (TARTRAZINE) (ARTIFICIAL COLORS). ALLERGY INFORMATION: WHEAT

Undeclared wheat.

Mar 18, 2026CNC Noodle Corporation

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