Estados Unidos Recalls

Retiros de seguridad del consumidor de la FDA, CPSC, NHTSA y USDA FSIS.

Showing 24 of 17,563 results
Food & BeverageUSFDA Food

Cake de Capuchino [image] Capuchino Cake The Original, Net Wt. 63 oz, packaged in a transparent and rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 824790850375

Galaxy RG Corp
FDA FoodClass II

Cake de Capuchino [image] Capuchino Cake The Original, Net Wt. 63 oz, packaged in a transparent and rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC 824790850375

Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

Jun 17, 2026Galaxy RG Corp
Medical DeviceUSFDA Devices

CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030

INSPIREMD Inc
FDA DevicesClass II

CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Jun 17, 2026INSPIREMD Inc
PharmaceuticalUSFDA Drugs

Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748-90); b) 1000 Capsules (51991-748-10), Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922.

Breckenridge Pharmaceutical, Inc.
FDA DrugsClass II

Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748-90); b) 1000 Capsules (51991-748-10), Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922.

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

Jun 17, 2026Breckenridge Pharmaceutical, Inc.
Food & BeverageUSFDA Food

DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRODUCT OF THAILAND Packed for: U.S. Trading Company Hayward, CA 94545-1130 UPC: 721557533567

U.S. Tov, Inc. dba U.S. Trading Company
FDA FoodClass II

DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRODUCT OF THAILAND Packed for: U.S. Trading Company Hayward, CA 94545-1130 UPC: 721557533567

Potential contamination with lead.

Jun 17, 2026U.S. Tov, Inc. dba U.S. Trading Company
Food & BeverageUSFDA Food

Flan Cake [image] Custard Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852959

Galaxy RG Corp
FDA FoodClass II

Flan Cake [image] Custard Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852959

Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

Jun 17, 2026Galaxy RG Corp
PharmaceuticalUSFDA Drugs

Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA. Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-644-30

Ascend Laboratories, LLC
FDA DrugsClass II

Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA. Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-644-30

Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis

Jun 17, 2026Ascend Laboratories, LLC
PharmaceuticalUSFDA Drugs

BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, Manufactured For: Beekeeper's Naturals USA Inc., Covina, CA 91789.

BEEKEEPER'S NATURALS USA INC.
FDA DrugsClass I

BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, Manufactured For: Beekeeper's Naturals USA Inc., Covina, CA 91789.

Microbial Contamination of Non-Sterile Products

Jun 17, 2026BEEKEEPER'S NATURALS USA INC.
Medical DeviceUSFDA Devices

Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320

Avanos Medical, Inc.
FDA DevicesClass II

Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Jun 17, 2026Avanos Medical, Inc.
Food & BeverageUSFDA Food

Marquesita de Guava [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706

Galaxy RG Corp
FDA FoodClass II

Marquesita de Guava [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706

Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

Jun 17, 2026Galaxy RG Corp
Food & BeverageUSFDA Food

Cheesecake de Guava [image] Guava Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790853116

Galaxy RG Corp
FDA FoodClass II

Cheesecake de Guava [image] Guava Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790853116

Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

Jun 17, 2026Galaxy RG Corp
Medical DeviceUSFDA Devices

Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction with the EXENT assays.

The Binding Site Group, Ltd.
FDA DevicesClass II

Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction with the EXENT assays.

It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured. The potential clinical hazards include false or missed detection of M-protein (false positive); and falsely elevated or decreased M-protein concentration.

Jun 17, 2026The Binding Site Group, Ltd.
Food & BeverageUSFDA Food

Taro Cakes UPC CODE #652565100055

E & S Grocery & Bakery Inc.
FDA FoodClass I

Taro Cakes UPC CODE #652565100055

Undeclared Egg Allergen

Jun 17, 2026E & S Grocery & Bakery Inc.
PharmaceuticalUSFDA Drugs

Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-133-85.

Zep Inc
FDA DrugsClass II

Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-133-85.

Microbial contamination of sterile products

Jun 17, 2026Zep Inc
PharmaceuticalUSFDA Drugs

Budesonide Inhalation Suspension, 1mg/2mL, 30 x 2 mL Sterile Single-Dose Ampules (5 Single-Dose Ampules per pouch, 6 pouches per carton, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited, Baska Ujeti Road, Ujeti Halol-289350, Gujarat, India, NDC 47335-633-49.

SUN PHARMACEUTICAL INDUSTRIES INC
FDA DrugsClass II

Budesonide Inhalation Suspension, 1mg/2mL, 30 x 2 mL Sterile Single-Dose Ampules (5 Single-Dose Ampules per pouch, 6 pouches per carton, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited, Baska Ujeti Road, Ujeti Halol-289350, Gujarat, India, NDC 47335-633-49.

Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution

Jun 17, 2026SUN PHARMACEUTICAL INDUSTRIES INC
Food & BeverageUSFDA Food

NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601

SENSORY SUPPLEMENT LLC
FDA FoodClass II

NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601

Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.

Jun 17, 2026SENSORY SUPPLEMENT LLC
Medical DeviceUSFDA Devices

Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.

Boston Scientific Corporation
FDA DevicesClass II

Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.

Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.

Jun 17, 2026Boston Scientific Corporation
Medical DeviceUSFDA Devices

Halyard, Towel Six Pack. Kit Code: AMTS70-01.

AVID Medical, Inc.
FDA DevicesClass II

Halyard, Towel Six Pack. Kit Code: AMTS70-01.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Jun 17, 2026AVID Medical, Inc.
PharmaceuticalUSFDA Drugs

Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-747-10

Breckenridge Pharmaceutical, Inc.
FDA DrugsClass II

Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-747-10

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

Jun 17, 2026Breckenridge Pharmaceutical, Inc.
Medical DeviceUSFDA Devices

Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940

INSPIREMD Inc
FDA DevicesClass II

Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Jun 17, 2026INSPIREMD Inc
Medical DeviceUSFDA Devices

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24

Avanos Medical, Inc.
FDA DevicesClass II

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Jun 17, 2026Avanos Medical, Inc.
Medical DeviceUSFDA Devices

Hintermann Series Talar Implant, Left, Size 2 REF 302112

DT MedTech, LLC
FDA DevicesClass II

Hintermann Series Talar Implant, Left, Size 2 REF 302112

Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.

Jun 17, 2026DT MedTech, LLC
Vehicle RecallUSNHTSA

Storyteller Overland - Alternator Pulley Failure May Cause Power Brakes and Power Steering Loss

Storyteller Overland
NHTSAELECTRICAL SYSTEM

Storyteller Overland - Alternator Pulley Failure May Cause Power Brakes and Power Steering Loss

An unexpected loss of power brakes increases the distance required to stop. A loss of power steering increases the amount of effort needed to control the vehicle. Both situations may increase the risk of a crash.

Jun 16, 2026Storyteller Overland
Vehicle RecallUSNHTSA

Forest River, Inc. - Incorrect GVWR on Certification Label/FMVSS 120

Forest River, Inc.
NHTSAEQUIPMENT

Forest River, Inc. - Incorrect GVWR on Certification Label/FMVSS 120

Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Jun 15, 2026Forest River, Inc.
Vehicle RecallUSNHTSA

Wabash National Corporation - Insufficient Rear Impact Protection/FMVSS 223

Wabash National Corporation
NHTSASTRUCTURE

Wabash National Corporation - Insufficient Rear Impact Protection/FMVSS 223

An improperly installed guard may not sufficiently protect a following vehicle, increasing the risk of injury during a rear end crash.

Jun 15, 2026Wabash National Corporation

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