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Food & Beverage
FDA FoodClass I

Al Yaman Halawa Extra Pistachio 907g (31.994 oz) plastic jars, UPC 5 287000 0980...

Product may be contaminated with Salmonella

Jun 24, 2026GREENWORLD FOOD EXPRESS (USA) LLC
Vehicle
NHTSAELECTRICAL SYSTEM

Elgin Sweeper Company - High Voltage Battery May Fail and Cause Fire

The defective batteries may overheat, increasing the risk of a fire.

Jun 24, 2026Elgin Sweeper Company
mamontessoribox - montessori hochets bois et crochet x2 pour bébés
RappelConsovolontaire (san...

mamontessoribox - montessori hochets bois et crochet x2 pour bébés

rapport d'essais du laboratoire administratif qui a rendu un avis : non conforme et dangereux,

Jun 24, 2026mamontessoribox
Medical Device
FDA DevicesClass II

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical T...

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
Vehicle
NHTSAGeneral Alert

Airstream, Inc. - Printed Circuit Board May Overheat

An overheated printed circuit board increases the risk of a fire.

Jun 24, 2026Airstream, Inc.
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as BASIC GYN, CW LAP GYN, D&C HYSTEROSC...

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

Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: P...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Vehicle
NHTSASTRUCTURE

Ford Motor Company - Fender Flare May Detach

A detached fender flare can become a road hazard and increase the risk of a crash.

Jun 24, 2026Ford Motor Company
Food & Beverage
Germany BVLGeneral Alert

Winter Outdoor Schuhe, schwarz

Gesundheitsschädliche Substanz

Jun 24, 2026Wünsche Fashion GmbH & Co.KG, Bei den Mühren 5, 20457 Hamburg
Vehicle
NHTSAPOWER TRAIN

Ford Motor Company - Vehicle Rollaway Risk

Park system damage may result in a vehicle rollaway, increasing the risk of a crash.

Jun 24, 2026Ford Motor Company
Food & Beverage
FDA FoodClass II

CANNOLI SICILIANI intended use: DESSERT condition: shelf stable shelf life: 12...

The product contains unapproved colors chlorophyll E140 and E141.

Jun 24, 2026MID DOLCIARIA SRL
Medical Device
FDA DevicesClass II

ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical ...

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
Food & Beverage
FDA FoodClass II

.155 CRUNCHY CANNOLI GLUTEN FREE intended use: DESSERT condition: shelf stable ...

The product contains unapproved colors chlorophyll E140 and E141.

Jun 24, 2026MID DOLCIARIA SRL
Food & Beverage
Germany BVLGeneral Alert

Henna Profix Black, 60 Gramm

Gesundheitsschädliche Substanz, Sonstige Gründe

Jun 24, 2026Inverkehrbringer: GT World of Beauty GmbH, Lützelhäuser Weg 14, 63571 Gelnhausen
Medical Device
FDA DevicesClass I

Description/REF: ACCESS TRAY/ASK-04001-JHH; ACCESS TRAY/ASK-04001-LMDTG; PI CVC ...

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
Vehicle
NHTSAGeneral Alert

Harbinger Motors Inc. - Loose Steering Gear Mounting Bolts

Broken or loose steering gear bolts can cause a loss of steering control, increasing the risk of a crash.

Jun 24, 2026Harbinger Motors Inc.
Medical Device
FDA DevicesClass II

BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A

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 I

Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B; SAC KIT: 18 GA X 12CM ...

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

MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK, Medline Kit Number...

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 Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL, Me...

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

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 II

MEDLINE Pre-connected Urethral Catheterization Tray and Bag, Red Rubber Latex, 1...

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: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103...

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

Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; ...

Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

Jun 24, 2026AMD Medicom Inc.
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