United States Recalls

Consumer recalls from the FDA, CPSC, NHTSA, and USDA FSIS.

Showing 24 of 16,529 results
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: TONSIL PACK CATH, 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
Pharmaceutical
FDA DrugsClass II

Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
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 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

ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical...

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
Medical Device
FDA DevicesClass I

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

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

Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catal...

Due to 11 volt Backup Battery failures.

Jun 24, 2026Thoratec LLC
Medical Device
FDA DevicesClass II

TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).

Jun 24, 2026Howmedica Osteonics Corp.
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
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT, Kit Uro Robot Cyst...

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

Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 unit...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Pharmaceutical
FDA DrugsClass II

Med Pride, Bacitracin Zinc Ointment, 1oz (28.3g) per tube, 72 tubes per case, Ma...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Pharmaceutical
FDA DrugsClass II

safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flav...

Defective container:may contain bottles with incomplete seals

Jun 24, 2026Keystone Industries
Pharmaceutical
FDA DrugsClass II

Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomyc...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
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
Pharmaceutical
FDA DrugsClass II

Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 1 oz (28.3g) tubes, Manufactured for...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Pharmaceutical
FDA DrugsClass II

Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride, syringe, IntegraDose Compoundi...

Subpotent Drug

Jun 24, 2026IntegraDose Compounding Services LLC
Medical Device
FDA DevicesClass II

Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHO...

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
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.
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
Medical Device
FDA DevicesClass II

Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM ...

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

Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K B...

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
Food & Beverage
FDA FoodClass I

White Cheddar Seasoning packed in the following sizes and configurations: 1. ...

Products were made with recalled California Dairies milk powder due to Salmonella.

Jun 24, 2026Jonco Industries
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: 1) CAROTID NEURO PACK, Medline Kit...

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
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