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. 3,026 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,026 in last 12 months

Showing 81818200 of 30,923 recalls

Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN):RLPC-35-180 ORDER...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RFSPC-35-180...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPW-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN)RFPC-35-180 ORDER...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System with Version 3.7.2 and below Recalled by...

The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RPC-35-180 Recalled...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· NuVasive Inc

Recalled Item: NuVasive MD Pulse III Multimodality System Pulse Software Recalled by...

The Issue: Due to an incorrect security key, customers were unable to connect to remote...

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

Class III — Low RiskOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System with Version 3.7.2 and below Recalled by...

The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2022· Becton Dickinson & Company

Recalled Item: BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System...

The Issue: Incorrect expiration date listed on the product labels. The expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Recalled by...

The Issue: Negative bias with patient samples. The mean patient sample bias range from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal limb holders: (1) DeRoyal Limb Holder Recalled by DeRoyal Industries...

The Issue: The webbing strap was laced improperly through the teeth of the buckle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2022· GE Healthcare, LLC

Recalled Item: (1) GE Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Inaccurate Distance and Area measurements with use of Global Stack viewport.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2022· Baxter Healthcare Corporation

Recalled Item: The Exacta-Mix 2400 compounding system Recalled by Baxter Healthcare...

The Issue: There is a potential for leaking valves on ports 1 to 4 in certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2022· Luminex Corporation

Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to SARS-CoV-2...

The Issue: SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect...

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

Class II — Potential Health HazardOngoing