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Medical Device
FDA DevicesClass II

Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All ...

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

Jun 24, 2026GE Medical Systems, LLC
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
Safety Alert
Health CanadaClass 2

Izem Energy brand “Boisson énergisante gazeuse” recalled due to labelling issues

Labelling and packaging

Jun 24, 2026CFIA
Medical Device
FDA DevicesClass I

Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC; PI JACC 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

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

Potential for overpressure alerts.

Jun 24, 2026ConMed Corporation
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
Medical Device
FDA DevicesClass II

Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SU...

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
Medical Device
FDA DevicesClass II

Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L

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

Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc 400 units, Neomycin Sulfa...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Food & Beverage
Germany BVLGeneral Alert

Haldi Powder, Kurkuma, 100 Gramm

Rückstände und Kontaminanten

Jun 24, 2026Hersteller: Gunarajan Handelsagentur, Seumestraße 8, 28197 Bremen Inverkehrbringer: Kreyenhop&Kluge GmbH& Co.KG, Industriestrasse 40, 28876 Oyten
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK, Medline Kit/S...

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 I

Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, A...

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
Germany BVLGeneral Alert

frischer Käse, 800 Gramm

Krankheitserreger

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

Medline convenience kits: DAVINCI MAIN DYNJ908031D

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: 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 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
Safety Alert
Health CanadaType II

Argon Medical Devices L-Cath™ PICC and Midline Catheters

Performance

Jun 24, 2026Medical devices
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: 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
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
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

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

Product tested positive for Salmonella

Jun 24, 2026International Food Products Corporation
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