Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,114 results
Medical DeviceUSFDA Devices

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Heart Cath Tray - RX, Part Number DDS1159B

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Heart Cath Tray - RX, Part Number DDS1159B

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.
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
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
Medical DeviceUSFDA Devices

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Block Tray - RX, Part Number AMS12414

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Block Tray - RX, Part Number AMS12414

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.
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
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
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

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
Food & BeverageFranceRappelConso

napoleon - poêle en fonte

napoleon
RappelConsovolontaire (san...

napoleon - poêle en fonte

ce produit ne satisfait pas aux exigences du règlement (ce) n°1935/2004.

Aug 5, 2026napoleon
Food & BeverageFranceRappelConso

les pensées sauvages - munster fermier les pensées sauvages

les pensées sauvages
RappelConsovolontaire (san...

les pensées sauvages - munster fermier les pensées sauvages

listeria

Aug 5, 2026les pensées sauvages
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 & BeverageFranceRappelConso

sans marque - morbier aop

sans marque
RappelConsovolontaire (san...

sans marque - morbier aop

détection de listeria innocua & listeria monocytogenes

Aug 5, 2026sans marque
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: Port Tray - RX, Part Number 008786-19

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port Tray - RX, Part Number 008786-19

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

Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory support for patients weighing more than 11lb (5kg) who require mechanical ventilation.

ResMed Ltd.
FDA DevicesClass I

Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory support for patients weighing more than 11lb (5kg) who require mechanical ventilation.

Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.

Aug 5, 2026ResMed Ltd.
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

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number AMS15517; 3) ENT Facial Pack, Pack Number AMS15863A.

Windstone Medical Packaging, Inc.
FDA DevicesClass II

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number AMS15517; 3) ENT Facial Pack, Pack Number AMS15863A.

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.
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
Food & BeverageAustraliaFSANZ Food

Key-Sun Kids Honey & Eucalyptus + acerola lozenge - 54 g (12 x 4.5 g lozenges)

Key-Sun Kids Honey & Eucalyptus + acerola lozenge
Key-Sun Kids Honey & Eucalyptus + acerola lozenge - 54 g (12 x 4.5 g lozenges)
FSANZ FoodFood Safety

Key-Sun Kids Honey & Eucalyptus + acerola lozenge - 54 g (12 x 4.5 g lozenges)

There is a risk of the presence of foreign matter (metal).

Aug 5, 2026Key-Sun Kids Honey & Eucalyptus + acerola lozenge
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

Medline Industries, LP Issues Nationwide Recall of Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits

Unknown Firm
RSS FeedGeneral Alert

Medline Industries, LP Issues Nationwide Recall of Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits

Aug 5, 2026
Medical DeviceUSFDA Devices

Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.

Stryker GmbH
FDA DevicesClass II

Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.

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

Aug 5, 2026Stryker GmbH
Medical DeviceUSFDA Devices

OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095

IsoTis OrthoBiologics, Inc.
FDA DevicesClass II

OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095

Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM (fill for 45 ¿ 11 mm configuration) instead of approx. 7.5 cc DBM (fill for 45 ¿ 17.5 mm configuration), which may lead to delayed fusion, incomplete fusion, pseudarthrosis, or lack of bone ingrowth.

Aug 5, 2026IsoTis OrthoBiologics, Inc.
Medical DeviceUSFDA Devices

Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity Premium Ingenuity CT Upgrades Ingenuity CT China Ingenuity Core 128 Elite Brazil

PHILIPS MEDICAL SYSTEMS
FDA DevicesClass II

Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity Premium Ingenuity CT Upgrades Ingenuity CT China Ingenuity Core 128 Elite Brazil

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

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