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. 2,989 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,989 in last 12 months

Showing 1274112760 of 56,506 recalls

Medical DeviceJuly 12, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...

The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
DrugJuly 11, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Defective Container: Tube split from side seam

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2022· WISSNER-BOSSERHOFF GMBH

Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...

The Issue: When the handset is disconnected from the power mains, and mains operation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2022· Intera Oncology, Inc.

Recalled Item: INTERA 3000 Hepatic Artery Infusion Pump Recalled by Intera Oncology, Inc....

The Issue: Higher than expected flow rate.

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

Class I — Serious Health HazardOngoing
DrugJuly 7, 2022· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...

The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 7, 2022· Refresco Beverages US Inc

Recalled Item: Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water...

The Issue: The product may contain trace amounts of coconut, which is not declared on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 7, 2022· Portland Specialty Baking LLC

Recalled Item: Lemon Muffins Recalled by Portland Specialty Baking LLC Due to Plastic material.

The Issue: Plastic material.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 7, 2022· OXFORD IMMUNOTEC LTD

Recalled Item: T-Cell Xtend .610 US Recalled by OXFORD IMMUNOTEC LTD Due to Due to...

The Issue: Due to equipment failure, affected products were stored at temperatures...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2022· OXFORD IMMUNOTEC LTD

Recalled Item: T-SPOT.TB .300 US Recalled by OXFORD IMMUNOTEC LTD Due to Due to equipment...

The Issue: Due to equipment failure, affected products were stored at temperatures...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2022· OXFORD IMMUNOTEC LTD

Recalled Item: AIM-V Medium .200/500 Recalled by OXFORD IMMUNOTEC LTD Due to Due to...

The Issue: Due to equipment failure, affected products were stored at temperatures...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2022· Olympus Corporation of the Americas

Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...

The Issue: Mis-wired component-the improperly wired component can result in additional...

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

Class II — Potential Health HazardOngoing
FoodJuly 6, 2022· Bumble Bee Foods, LLC

Recalled Item: Bumble Bee Smoked Clams Shucked Easy Open NET WT. 3.75 Recalled by Bumble...

The Issue: Detectable levels of Per- and polyfluoroalkyl substances (PFAS).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 34033-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund