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. 2,654 recalls have been distributed to California in the last 12 months.
Showing 50661–50680 of 56,506 recalls
Recalled Item: IBU (TM) IBUPROFEN Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Labeling: Incorrect or missing lot and/or exp date- This product is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...
The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blythedale Farm Camembert Vermont Recalled by Blythedale Farm Inc. Due to...
The Issue: Inadequate pasteurization
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blythedale Farm Farmstead Brie Recalled by Blythedale Farm Inc. Due to...
The Issue: Inadequate pasteurization
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blythedale Farm Vermont Brie Recalled by Blythedale Farm Inc. Due to...
The Issue: Inadequate pasteurization
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...
The Issue: It was discovered that Carestream received a report from a customer that 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composite Series Skull Clamp Recalled by Integra LifeSciences Corp. Due to...
The Issue: An investigation of an adverse trend of complaints for the Skull Clamp index...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code:...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...
The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.