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 95019520 of 30,923 recalls

Medical DeviceAugust 27, 2021· North Coast Medical Inc

Recalled Item: Norco Ultrasound Gel Recalled by North Coast Medical Inc Due to Ultrasound...

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 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Pioneer nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: Optima MR450w 1.5T nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: 1.5T SIGNA HDxt MR System nuclear magnetic resonance imaging system Recalled...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Architect nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Creator Recalled by GE Healthcare, LLC Due to Under certain...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: Discovery MR750w 3.0T nuclear magnetic resonance imaging system Recalled by...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Voyager nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Artist nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: Discovery MR750 3.0T nuclear magnetic resonance imaging system Recalled by...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· GE Healthcare, LLC

Recalled Item: SIGNA Premier nuclear magnetic resonance imaging system Recalled by GE...

The Issue: Under certain conditions, some slices may be missing which can lead to a gap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2021· Atrium Medical Corporation

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Instrumentation Laboratory

Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...

The Issue: Labeled On-board instrument stability issue for current and future lots,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Atrium Medical Corporation

Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...

The Issue: The product package may potentially contain a mismatched graft that does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Accelerated Care Plus Corporation

Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...

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 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing