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. 2,669 recalls have been distributed to California in the last 12 months.
Showing 41561–41580 of 56,506 recalls
Recalled Item: TESTOSTERONE Recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLUTATHIONE MDV Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHORIONIC GONADOTROPIN Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METHYLCOBALAMIN MDV Recalled by JD & SN Inc., dba Moses Lake Professional...
The Issue: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADRUCIL (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Presence of Particulate Matter: silcone rubber and fluorouracil crystals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: univasc (moexipril HCl) tablets Recalled by Ucb, Inc Due to Failed...
The Issue: Failed Dissolution Testing: Failed 24 month dissolution testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nisoldipine Extended Release Tablets Recalled by Shionogi Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray...
The Issue: Defective Delivery System: Inhalers do not spray properly, emitting either...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cold Smoked Salmon Deli trays (CS300) Recalled by Certified Smoked Fish LLC...
The Issue: Certified Smoked Fish is Cold Smoked Salmon because they have the potential...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cold Smoked Salmon Trim (CST50) Recalled by Certified Smoked Fish LLC Due to...
The Issue: Certified Smoked Fish is Cold Smoked Salmon because they have the potential...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due...
The Issue: EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Unity Z3D software. Merge Unity PACS (formerly DR Systems Recalled by...
The Issue: The software is unable to accurately determine the calcium score of scans...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips GoSafe Mobile Help Button Recalled by Lifeline Systems, Incorporated...
The Issue: Irregular battery disconnection resulted in issues with Mobile Health Button...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC) Recalled by...
The Issue: customers are receiving a high number of Abnormal Assay Errors or are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare TraumaDiagnost Recalled by Philips Electronics North...
The Issue: If arm is not fastened securely it could fall down.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft...
The Issue: Biomet has initiated a recall on Biomet Spine Lineum OCC Starter Flexible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Pioneer Plus Re-Entry Catheter Recalled by Volcano Corporation Due...
The Issue: Due to a manufacturing defect, there is the possibility that a small wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER ISOTON 4 Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER LH Series Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument for Sternal ZIPFIX Recalled by Synthes (USA)...
The Issue: The end cap may loosen and detach making the instrument non-functional. No...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.