Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,114 results
Safety AlertUSCPSC

Magnetic Fidget Sliders Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys: Sold on Amazon by BUSOHA

Unknown Firm
Magnetic Fidget Sliders Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys: Sold on Amazon by BUSOHA
CPSCGeneral Alert

Magnetic Fidget Sliders Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys: Sold on Amazon by BUSOHA

The magnetic fidget sliders violate the mandatory standard for toys because they can liberate loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Aug 6, 2026
Food & BeverageFranceRappelConso

sans marque - escalopes de dinde crues marinées

sans marque
RappelConsovolontaire (san...

sans marque - escalopes de dinde crues marinées

présence de salmonelle typhimurium

Aug 6, 2026sans marque
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
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
Medical DeviceUSFDA Devices

Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades

PHILIPS MEDICAL SYSTEMS
FDA DevicesClass II

Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades

The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the clinical acquisition being inadequate for diagnosis, causing a potential for patient rescan and receiving additional radiation.

Aug 5, 2026PHILIPS MEDICAL SYSTEMS
Medical DeviceUSFDA Devices

Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150.

Stryker GmbH
FDA DevicesClass II

Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150.

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

Aug 5, 2026Stryker GmbH
Medical DeviceUSFDA Devices

Brand Name: GEM Premier 7000 with iQM3 Product Name: GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Intelligent Quality Management 3 (iQM3) is used as the quality control (QC) and assessment system for the GEM Premier 7000. portable blood analyzer

Instrumentation Laboratory
FDA DevicesClass II

Brand Name: GEM Premier 7000 with iQM3 Product Name: GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Intelligent Quality Management 3 (iQM3) is used as the quality control (QC) and assessment system for the GEM Premier 7000. portable blood analyzer

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
Food & BeverageFranceRappelConso

sans marque - crevettes grises cuites

sans marque
RappelConsovolontaire (san...

sans marque - crevettes grises cuites

présence de listéria

Aug 5, 2026sans marque
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.
Medical DeviceUSFDA Devices

M5 Corpus Power Wheelchair REF,120032

Permobil Inc
FDA DevicesClass II

M5 Corpus Power Wheelchair REF,120032

This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in certain circumstances.

Aug 5, 2026Permobil Inc
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
Safety AlertUSRSS Feed

Sun Noodle Issues Voluntary Recall of Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base Due to Undeclared Fish Allergen

Unknown Firm
RSS FeedGeneral Alert

Sun Noodle Issues Voluntary Recall of Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base Due to Undeclared Fish Allergen

Aug 5, 2026
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
Medical DeviceUSFDA Devices

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr Fred Chiu Single Shot Epi Tray - Rx, Part Number AMS1095(E ; 2) Single Shot Epidural Tray - RX, Part Number AMS11296A; 3) Nerve Block Tray - RX, Part Number AMS11314A; 4) Epidural Tray - RX, Part Number AMS11910A; 5) Nerve Block Tray - RX, Part Number AMS12171; 6) Single Shot Epidural Tray - RX, Part Number AMS12219A; 7) Universal Block Tray - RX, Part Number AMS12381B.

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr Fred Chiu Single Shot Epi Tray - Rx, Part Number AMS1095(E ; 2) Single Shot Epidural Tray - RX, Part Number AMS11296A; 3) Nerve Block Tray - RX, Part Number AMS11314A; 4) Epidural Tray - RX, Part Number AMS11910A; 5) Nerve Block Tray - RX, Part Number AMS12171; 6) Single Shot Epidural Tray - RX, Part Number AMS12219A; 7) Universal Block Tray - RX, Part Number AMS12381B.

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.
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
Medical DeviceUSFDA Devices

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio Pack - RX, Part Number AMS9461

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio Pack - RX, Part Number AMS9461

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

Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number: 00024019255 Portable blood analyzer system

Instrumentation Laboratory
FDA DevicesClass II

Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number: 00024019255 Portable blood analyzer system

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
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

aucune - crevette cuite refrigeree 20/30 p. notialis sauvage op 2kg

aucune
RappelConsovolontaire (san...

aucune - crevette cuite refrigeree 20/30 p. notialis sauvage op 2kg

détection de listeria monocytogenes dans un produit

Aug 5, 2026aucune
PharmaceuticalUSFDA Drugs

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro Labs Limited, India, Manufactured for: Micro Labs USA Inc., Somerset, NJ 08873. NDC 42571-147-26.

MICRO LABS USA INC
FDA DrugsClass II

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro Labs Limited, India, Manufactured for: Micro Labs USA Inc., Somerset, NJ 08873. NDC 42571-147-26.

Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.

Aug 5, 2026MICRO LABS USA INC
Food & BeverageFranceRappelConso

simond - dégaines alpinism & vertika

simond
RappelConsovolontaire (san...

simond - dégaines alpinism & vertika

nous avons identifié un défaut sur le rivetage du doigt fil de votre dégaine. ce défaut d'assemblage peut entraîner la rupture du doigt fil et engendrer un risque de casse du mousqueton en cas de chute.

Aug 5, 2026simond
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

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 & 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

Install The Recall File App

Check safety warnings, scan your pantry, and monitor your vehicles directly from your home screen.