Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,267 results
Pharmaceutical
FDA DrugsClass II

Circle K, triple antibiotic ointment, Bacitracin Zinc (400 units), Neomycin Sulf...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Pharmaceutical
FDA DrugsClass II

Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Ca...

Crystallization; identified as Buprenorphine free base

Jun 24, 2026Par Health USA, LLC
Pharmaceutical
FDA DrugsClass II

Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Conten...

Defective container:may contain bottles with incomplete seals

Jun 24, 2026Keystone Industries
Medical Device
FDA DevicesClass I

Description/REF: ACCESS TRAY/ASK-04001-MC3

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 convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B

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
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

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

Due to 11 volt Backup Battery failures.

Jun 24, 2026Thoratec LLC
Pharmaceutical
FDA DrugsClass II

Med Pride, Bacitracin Zinc Ointment, 500 units, 0.9g packets Net Wt 130g, 144 co...

CGMP Deviations; deficiencies observed during FDA inspection

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

Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y ...

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: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3...

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

Medtronic O-arm O2 Imaging System. Model Number: BI70002000.

Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.

Jun 24, 2026Medtronic Navigation, Inc.-Boxborough
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.
Pharmaceutical
FDA DrugsClass II

VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Act...

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

Jun 24, 2026PAI Holdings LLC
Medical Device
FDA DevicesClass I

Description/REF: PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2; PI CVC KIT:...

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: PELVIC LAP 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

ALYON Surgical Lighting System

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

Jun 24, 2026Steris Corporation
Medical Device
FDA DevicesClass I

Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-00...

Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

Jun 24, 2026Datex-Ohmeda Inc
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT ...

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 Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 14 Fr...

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: DISCECTOMY PACK DYNJ86476B EAR DYNJ81460C DYN...

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

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 II

Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A ...

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
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