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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
Medical Device
FDA DevicesClass I

Description/REF: PARACENTESIS KIT/ASK-00376-JHH

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) CV DRAPING/BASIN, Medline Kit N...

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, Bacitracin Zinc Ointment, 500 units, 1oz (28.3g) tubes, Manufactured ...

CGMP Deviations; deficiencies observed during FDA inspection

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

Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L

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: PSI KIT: 7 FR X 4 IN/ASK-09701-UP; PSI KIT: 8.5 FR X 4 1/8 IN (...

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
FDA FoodClass II

Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags

Product tested positive for Salmonella

Jun 24, 2026International Food Products Corporation
Pharmaceutical
FDA DrugsClass II

Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc (400 units), Neomyci...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
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

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical ...

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
Pharmaceutical
FDA DrugsClass II

VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Acti...

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

Jun 24, 2026PAI Holdings LLC
Food & Beverage
Germany BVLGeneral Alert

frischer Käse, 800 Gramm

Krankheitserreger

Jun 24, 2026Käse King Lessingstraße 16 99510 Apolda
Medical Device
FDA DevicesClass I

Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F; HEMODIALYS...

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
Pharmaceutical
FDA DrugsClass II

Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30...

Defective container:may contain bottles with incomplete seals

Jun 24, 2026Keystone 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
Pharmaceutical
FDA DrugsClass II

Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc (equivalent to 400 units)...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Food & Beverage
FDA FoodClass II

Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies...

Undeclared melatonin.

Jun 24, 2026Dkiru LLC
Medical Device
FDA DevicesClass II

Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716

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

Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery, ABT Model/Ca...

Due to 11 volt Backup Battery failures.

Jun 24, 2026Thoratec LLC
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