Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,114 results
Medical DeviceUSFDA Devices

EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77722

Medtronic Perfusion Systems
FDA DevicesClass II

EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77722

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.

Aug 5, 2026Medtronic Perfusion Systems
Food & BeverageUSFDA Food

Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is handwritten in black marker on the top lid of the clamshell package. No lot code or UPC.

Nelson & Isa Lacteos LLC
FDA FoodClass I

Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is handwritten in black marker on the top lid of the clamshell package. No lot code or UPC.

Products may be contaminated with Listeria monocytogenes.

Aug 5, 2026Nelson & Isa Lacteos LLC
Medical DeviceUSFDA Devices

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Part Number AMS10411B; 2) ENT Pack, Part Number AMS10411C; 3) Rhinoplasty Pack, Part Number AMS11963A; 4) Spine Pack, Part Number AMS12636C; 5) Lumbar Lami Pack, Part Number AMS12731; 6) Septoplasty Pack, Part Number AMS13150; 7) Septoplasty Pack, Part Number AMS13150A; 8) Septoplasty Pack, Part Number AMS13150B; 9) Rhinoplasty Pack, Part Number AMS14496A; 10) Rhinoplasty Pack, Part Number AMS14496B; 11) Rhinoplasty Pack, Part Number AMS14496C; 12) Laryngoscopy Pack, Part Number AMS14736; 13) Nasal and Sinus Pack, Part Number AMS16417; 14) Major Pack, Part Number AMS16586; 15) Major Pack, Part Number AMS16586A; 16) Nasal and Sinus Pack, Part Number AMS7619A; 17) Sinus Pack, Part Number AMS7819A.

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Part Number AMS10411B; 2) ENT Pack, Part Number AMS10411C; 3) Rhinoplasty Pack, Part Number AMS11963A; 4) Spine Pack, Part Number AMS12636C; 5) Lumbar Lami Pack, Part Number AMS12731; 6) Septoplasty Pack, Part Number AMS13150; 7) Septoplasty Pack, Part Number AMS13150A; 8) Septoplasty Pack, Part Number AMS13150B; 9) Rhinoplasty Pack, Part Number AMS14496A; 10) Rhinoplasty Pack, Part Number AMS14496B; 11) Rhinoplasty Pack, Part Number AMS14496C; 12) Laryngoscopy Pack, Part Number AMS14736; 13) Nasal and Sinus Pack, Part Number AMS16417; 14) Major Pack, Part Number AMS16586; 15) Major Pack, Part Number AMS16586A; 16) Nasal and Sinus Pack, Part Number AMS7619A; 17) Sinus Pack, Part Number AMS7819A.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.

Aug 5, 2026Windstone Medical Packaging, Inc.
Medical DeviceUSFDA Devices

Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.

Stryker GmbH
FDA DevicesClass II

Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Aug 5, 2026Stryker GmbH
Food & BeverageFranceRappelConso

sans marque - andouille de dinan

sans marque
RappelConsovolontaire (san...

sans marque - andouille de dinan

présence de listeria monocytogenes

Aug 5, 2026sans marque
Food & BeverageUSFDA Food

Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3

Mellish Island Corp
FDA FoodClass II

Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3

Firm's finished product label does not declare the source of marine collagen which was determined to be fish.

Aug 5, 2026Mellish Island Corp
Medical DeviceUSFDA Devices

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Nerve Block Tray - RX, Part Number AMS13975A; 2) Universal Block Tray- RX, Part Number AMS2009; 3) Nerve Block Tray - RX, Part Number AMS3224.

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Nerve Block Tray - RX, Part Number AMS13975A; 2) Universal Block Tray- RX, Part Number AMS2009; 3) Nerve Block Tray - RX, Part Number AMS3224.

Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier quality issues.

Aug 5, 2026Windstone Medical Packaging, Inc.
Medical DeviceUSFDA Devices

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

Permobil Inc
FDA DevicesClass II

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,

Aug 5, 2026Permobil Inc
Medical DeviceUSFDA Devices

Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.

Stryker GmbH
FDA DevicesClass II

Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Aug 5, 2026Stryker GmbH
PharmaceuticalUSFDA Drugs

Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-00.

MYLAN PHARMACEUTICALS INC
FDA DrugsClass II

Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-00.

Presence of precipitate

Aug 5, 2026MYLAN PHARMACEUTICALS INC
Medical DeviceUSFDA Devices

Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.

Stryker GmbH
FDA DevicesClass II

Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Aug 5, 2026Stryker GmbH
Food & BeverageFranceRappelConso

nissan - qashqai voiture particulière

nissan
RappelConsoGeneral Alert

nissan - qashqai voiture particulière

pendant le fonctionnement du moteur, la conduite de carburant peut se déplacer à l'intérieur de son clip de retenue dans le compartiment moteur. ce mouvement pourrait endommager la conduite de carburant et provoquer une fuite de carburant, créant un risque d'incendie.

Aug 5, 2026nissan
Vehicle RecallUSNHTSA

Tesla, Inc. - Low Beam Headlights May Be Too Bright/FMVSS 108

Tesla, Inc.
NHTSAEXTERIOR LIGHTING

Tesla, Inc. - Low Beam Headlights May Be Too Bright/FMVSS 108

Headlight low beams that are too bright can reduce visibility for oncoming drivers, increasing the risk of a crash.

Aug 5, 2026Tesla, Inc.
PharmaceuticalUSFDA Drugs

Dabigatran Etexilate Capsules, 75 mg, 30-count (3x10) blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268, NDC 0904-7253-04.

Ascend Laboratories, LLC
FDA DrugsClass III

Dabigatran Etexilate Capsules, 75 mg, 30-count (3x10) blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268, NDC 0904-7253-04.

Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability

Aug 5, 2026Ascend Laboratories, LLC
Safety AlertUSRSS Feed

Victory Medical Center Pharmacy Issues Voluntary Nationwide Recall of Certain Lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials Due to Elevated Endotoxin Levels

Unknown Firm
RSS FeedGeneral Alert

Victory Medical Center Pharmacy Issues Voluntary Nationwide Recall of Certain Lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials Due to Elevated Endotoxin Levels

Aug 5, 2026
Food & BeverageFranceRappelConso

sans marque - friton de porc

sans marque
RappelConsovolontaire (san...

sans marque - friton de porc

présence de listeria monocytogenes (agent responsable de la listériose)

Aug 5, 2026sans marque
Food & BeverageFranceRappelConso

sans marque - crevettes grises cuites

sans marque
RappelConsovolontaire (san...

sans marque - crevettes grises cuites

présence de listéria

Aug 5, 2026sans marque
Food & BeverageFranceRappelConso

andré cazaux - saucisson sec andré cazaux , saucisson sec le montagnard

andré cazaux
RappelConsovolontaire (san...

andré cazaux - saucisson sec andré cazaux , saucisson sec le montagnard

présence de salmonelle

Aug 5, 2026andré cazaux
Food & BeverageGermanyGermany BVL

verschiedene Yopokki Rice-Cake-Becher

TJX Deutschland Ltd. & Co. KG, Peter-Mueller-Str. 18, 40468 Düsseldorf
Germany BVLGeneral Alert

verschiedene Yopokki Rice-Cake-Becher

Krankheitserreger

Aug 5, 2026TJX Deutschland Ltd. & Co. KG, Peter-Mueller-Str. 18, 40468 Düsseldorf
Food & BeverageFranceRappelConso

u bio - petits pois carottes u bio sachet surgelé 600g

u bio
RappelConsovolontaire (san...

u bio - petits pois carottes u bio sachet surgelé 600g

non conformite microbiologique

Aug 5, 2026u bio
Medical DeviceUSFDA Devices

GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Portable blood analyzer system. Affected Accessory: Bar Code Reader (BCR) Wand Part No. 00024015859

Instrumentation Laboratory
FDA DevicesClass II

GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Portable blood analyzer system. Affected Accessory: Bar Code Reader (BCR) Wand Part No. 00024015859

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Aug 5, 2026Instrumentation Laboratory
Safety AlertAustraliaAustralia Products

Secret diary pen with UV light

Unknown Firm
Secret diary pen with UV light
Australia ProductsButton batteries

Secret diary pen with UV light

The pen doesn’t comply with the mandatory standards for products containing button/coin batteries . The battery isn’t secured, and children could access the button/coin battery.

Aug 5, 2026
Medical DeviceUSFDA Devices

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522

Medtronic Perfusion Systems
FDA DevicesClass II

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.

Aug 5, 2026Medtronic Perfusion Systems
Food & BeverageFranceRappelConso

auchan - auchan sh strie 6x100g (auchan et prix bas)

auchan
RappelConsovolontaire (san...

auchan - auchan sh strie 6x100g (auchan et prix bas)

défaut de fabrication, défaut d'étanchéité (ex: micro fuites, thermoscellage défectueux) ou anomalies de conditionnement¤

Aug 5, 2026auchan

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