Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 3,022 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,022 in last 12 months

Showing 95219540 of 30,923 recalls

Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch Recalled by...

The Issue: Potential for difficulty in safety mechanism activation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch Recalled by...

The Issue: Potential for difficulty in safety mechanism activation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Bard Peripheral Vascular Inc

Recalled Item: Catalog # BEK4511 Recalled by Bard Peripheral Vascular Inc Due to Due to...

The Issue: Due to misbranded products shipped to customers.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Bard Peripheral Vascular Inc

Recalled Item: Catalog # BEK3411 Recalled by Bard Peripheral Vascular Inc Due to Due to...

The Issue: Due to misbranded products shipped to customers.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2021· Aesthetics Systems Usa Inc

Recalled Item: Action De Gala Recalled by Aesthetics Systems Usa Inc Due to Ultrasound gels...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 20, 2021· ConvaTec, Inc

Recalled Item: DuoDERM Control Gel Formula Border Dressings 15x15cm (1x5pk) Recalled by...

The Issue: Primary packaging labeling may be incorrect.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Microbiologics Inc

Recalled Item: SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use...

The Issue: The SARS-CoV-2 Process Control (Pellet) contains RNA transcripts that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Greiner Bio-One North America, Inc.

Recalled Item: Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate Recalled...

The Issue: Complaint of tubes clotting due to variation of anticoagulant and/or tubes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Microbiologics Inc

Recalled Item: SARS-CoV-2 Process Control (Swab) - Product Usage: intended for use Recalled...

The Issue: The product indicated is contaminated with a plasmid DNA that contains the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2021· Fort Defiance Industries, LLC

Recalled Item: P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641 Recalled by...

The Issue: The rear heater plate and cover assembly that contains the electrical wiring...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2021· Philips Ultrasound Inc

Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...

The Issue: Battery system data issue with the ultrasound system can intermittently...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2021· Philips Ultrasound Inc

Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...

The Issue: Battery system data issue with the ultrasound system can intermittently...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing