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. 3,040 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,040 in last 12 months

Showing 61016120 of 56,506 recalls

DrugMay 17, 2024· GlaxoSmithKline LLC

Recalled Item: Tivicay PD (dolutegravir) 5mg Tablets for Oral Suspension Recalled by...

The Issue: Labeling: Incorrect Lot and/or Expiration Date: The carton has incorrect...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 17, 2024· Cadwell Industries Inc

Recalled Item: Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to...

The Issue: Electroneurodiagnostic medical device may contain a defective printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...

The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...

The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System Recalled by...

The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Siemens Healthcare Diagnostics Inc

Recalled Item: Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Recalled by...

The Issue: Siemens Healthineers has identified an issue with the RAPIDPoint500e system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Biomet, Inc.

Recalled Item: RingLoc Bi-Polar Hip System Acetabular Cup Recalled by Biomet, Inc. Due to...

The Issue: 41 mm acetabular outer heads were potentially assembled with a 42 mm locking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for...

The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
FoodMay 16, 2024· Breadbox Co.

Recalled Item: Breadman Raisin Bread Recalled by Breadbox Co. Due to Undeclared Milk

The Issue: Undeclared milk allergen and undeclared Yellow No. 5

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2024· Breadbox Co.

Recalled Item: Breadman Brioche products in plastic bags: Brioche Toast Recalled by...

The Issue: Undeclared Yellow No. 5

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2024· Breadbox Co.

Recalled Item: Breadman Jalapeno Cheese Bagels Recalled by Breadbox Co. Due to Undeclared Milk

The Issue: Undeclared milk allergen

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Estradiol Transdermal System Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugMay 16, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Estradiol Transdermal System Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugMay 16, 2024· Rising Pharma Holding, Inc.

Recalled Item: Pregabalin Capsules 50mg Recalled by Rising Pharma Holding, Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules: Complaint received from a re-packager,...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 16, 2024· Medtronic Perfusion Systems

Recalled Item: TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion...

The Issue: Incorrect component placed in four manufactured lots of the TourniKwik"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel (30 test kit) Recalled by...

The Issue: Due to increase of false positive Vibrio/Vibrio Cholerae results when using...

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

Class II — Potential Health HazardOngoing