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. 3,068 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,068 in last 12 months

Showing 28612880 of 30,923 recalls

Medical DeviceOctober 24, 2024· GE Healthcare (China) Co., Ltd.

Recalled Item: GE Proteus XR/A radiographic system Recalled by GE Healthcare (China) Co.,...

The Issue: Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· Micro-X Ltd.

Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to During...

The Issue: During internal testing it was found that if the system is Ready to expose...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Lab Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE COLLECTION VHC Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Clean Catch Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE KIT W/BD CUP Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: UA KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Specimen...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: URINALYSIS KIT 4 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Specimen container included in kits is labeled as sterile, but has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2024· Micro-X Ltd.

Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Mobile...

The Issue: Mobile x-ray system receiving/storage(operation) requirements to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2024· ICU Medical, Inc.

Recalled Item: Allegedly counterfeit batteries manufactured by CSB batteries being used...

The Issue: ICU Medical has received reports of allegedly counterfeit CSB batteries...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica¿ CH ¿2-Microglobulin (B2M) - In vitro diagnostic use in Recalled by...

The Issue: Potential for falsely depressed auto-diluted results for samples above the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Atellica CH Reaction Ring Cuvette Segment-has cuvettes that contain...

The Issue: A manufacturing defect causes Atellica CH Reaction Ring Cuvette Segments...

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

Class II — Potential Health HazardOngoing