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Medical Device
FDA DevicesClass I

Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB; AGBA PI...

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass II

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-...

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
Pharmaceutical
FDA DrugsClass II

DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Man...

Defective container:may contain bottles with incomplete seals

Jun 24, 2026Keystone Industries
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT, AS...

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ6...

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

iLet Bionic Pancreas, REF: BB1001

The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfully slides the unlock slider on the Lock Screen, no screen transition occurs, and the user remains on the Lock Screen. Because the user cannot exit the Lock Screen, the user is unable to perform a cartridge change or meal announcement. If this occurs and therapy is in progress, therapy will continue normally until the insulin cartridge is depleted. The user will be unable to perform a cartridge change or a meal announcement and will be stuck on the screen until the battery fully drains. This can lead to hyperglycemia.

Jun 24, 2026Beta Bionics, Inc.
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK, Medline Kit Numbe...

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Pharmaceutical
FDA DrugsClass II

Med Pride, 1% Clotrimazole Antifungal Cream, Net Wt. 1oz (28.3g), Manufactured f...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Medical Device
FDA DevicesClass II

Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire stimulation Lea...

Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By Date may result in unplanned or premature revision surgery.

Jun 24, 2026Inspire Medical Systems Inc.
Medical Device
FDA DevicesClass I

Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A; AM/AT PI MID...

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Food & Beverage
UK FSAPublished

Morrisons recalls Morrisons Coronation Chicken Pasta because of undeclared milk

Milk This product may contain milk making it a possible health risk for anyone with an allergy to milk or intolerance to milk or milk constituents.

Jun 24, 2026Morrisons
Medical Device
FDA DevicesClass II

ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Cata...

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
Pharmaceutical
FDA DrugsClass II

PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavo...

Defective container:may contain bottles with incomplete seals

Jun 24, 2026Keystone Industries
Vehicle
NHTSAEQUIPMENT ADAPT...

Ricon Corporation - Wheelchair Lift May Inadvertently Move

A wheelchair lift that continues to move while occupied increases the risk of injury.

Jun 23, 2026Ricon Corporation
Vehicle
NHTSAELECTRICAL SYSTEM

Rockford Corporation - Inadequate Fuse Protection

Inadequate protection may increase the risk of a fire.

Jun 23, 2026Rockford Corporation
Vehicle
NHTSAGeneral Alert

General Motors, LLC - Improperly Tightened Steering Gear Assembly Nut

A loose nut that separates from the steering gear assembly while driving can cause a loss of steering control, increasing the risk of a crash.

Jun 23, 2026General Motors, LLC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026302 - GENERAL MOTORS

Seats And Restraints

Jun 23, 2026TC
Food & Beverage
RappelConsoGeneral Alert

shooting ducks battle edition jeu de tir

le jouet a de petites pièces facilement détachables (balles en mousse) qui peuvent facilement se détacher. un petit enfant peut les mettre dans leur bouche et s'étouffer. le compartiment à piles peut facilement être ouvert sans utiliser d'outils et les piles bouton à l'intérieur sont facilement accessibles. un enfant peut les mettre dans la bouche et les avaler, ce qui pourrait endommager son tractus gastro-intestinal et/ou l’étouffer.

Jun 23, 2026
Food & Beverage
RappelConsoGeneral Alert

black small electric hot pot multi-function pot chaud électrique

le conducteur interne du produit peut surchauffer. comme ce conducteur touche la paroi métallique du produit, l'utilisateur peut le toucher et subir des brûlures.

Jun 23, 2026
Food & Beverage
RappelConsoGeneral Alert

hair dryer sèche-cheveux

en cas d'obstruction de l'entrée d'air, le produit peut surchauffer et fondre et provoquer un incendie.

Jun 23, 2026
Food & Beverage
RappelConsoGeneral Alert

bébé cacahuète torsion voiture infantile voiture-jouet à roulettes

le jouet devient lâche lors de l'utilisation, créant un espace entre la roue gauche et le corps du jouet. un enfant pourrait piéger ses doigts dans cet espace et se blesser. en outre, le sac en plastique de l'emballage est trop mince. si un enfant joue avec, le plastique peut couvrir la bouche et le nez, provoquant l'étouffement de l'enfant.

Jun 23, 2026
Food & Beverage
RappelConsoGeneral Alert

coton bébé wrap transporteur nouveau-né écharpe pour bébé

l'écharpe pour bébé n'a pas les instructions requises pour une utilisation correcte. cela pourrait conduire à un enfant ne pas être correctement fixé dans le porte-bébé, ou le produit mal réglé, ce qui pourrait faire tomber le bébé et subir des blessures.

Jun 23, 2026
Food & Beverage
RappelConsoGeneral Alert

adaptater adaptateur de puissance

les distances et la protection entre les circuits primaires et secondaires sont insuffisantes, ce qui pourrait provoquer un choc électrique.

Jun 23, 2026
Food & Beverage
Germany BVLGeneral Alert

Chio „Dip! Hot Cheese“ mit der Etikettierung "Dip! Hot Salsa"

Allergene

Jun 23, 2026Intersnack Deutschland SE, Erna-Scheffler-Straße 3, 51103 Köln
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