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. 2,839 recalls have been distributed to California in the last 12 months.
Showing 25701–25720 of 56,506 recalls
Recalled Item: ARCHITECT MAGNESIUM Recalled by Abbott Laboratories, Inc Due to Abbott...
The Issue: Abbott internal testing has identified that the Magnesium urine application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQF Red Raspberries Recalled by Willamette Valley Pie Company, LLC. Due to...
The Issue: IQF Red Raspberries are recalled due to a potential contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Curity All Purpose Sponges Recalled by Cardinal Health 200, LLC Due to...
The Issue: Curity All Purpose Sponges were not sterilized and distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexima Duodenal Bend Biliary Stent with Delivery System Recalled by Boston...
The Issue: The sterile barrier may contain packaging seal defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vergene Amplification Tray - 700uL Recalled by Luminex Corporation Due to On...
The Issue: On lot of VERIGENE(R) BC-GP Utility Kits (20-011-018) were labeled with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Loading Car Recalled by Steris Corporation Due to The ATLAS loading...
The Issue: The ATLAS loading car may not remain fully engaged with the latch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexima Duodenal Bend Biliary Stent with Delivery System Recalled by Boston...
The Issue: The sterile barrier may contain packaging seal defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse(TM) Treatment Planning System with Proton Convolution Superposition...
The Issue: There is an anomaly with the Eclipse(TM) Treatment Planning System [TPS]...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips Medical Systems Nederlands...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia WT(P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P) 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to The products...
The Issue: The products were manufactured with longer than specified sheaths.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T High Performance Recalled by Philips Medical Systems Nederlands...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.