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 48961–48980 of 56,506 recalls
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...
The Issue: Covidien is conducting a voluntary field corrective action on Puritan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pyridostigmine Bromide Tablets USP Recalled by Corepharma LLC Due to Failed...
The Issue: Failed Dissolution Specification: Corepharma Inc. is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LONG AID Curl Activator Gel Recalled by Keystone Laboratories Inc Due to...
The Issue: Product has a cloudy appearance
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresh Cactus ("Nopal") Recalled by Marquez Produce Inc. Due to Marquez...
The Issue: Marquez Produce is recalling Fresh Cactus because of unapproved pesticides.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hnos. Perez brand cactus leaves (pads): distributed by: West Coast Recalled...
The Issue: State of California, Department of Pesticide Regulation samples Cactus Pads...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...
The Issue: Ensuring all customers have the tools to assist in verifying the setting of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuperElastic Regular force NiTi lower or upper Natural arches. 0.14 Recalled...
The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 Recalled...
The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: King Systems KLTSD414 Quantity Recalled by King Systems Corp. Due to KLTD214...
The Issue: KLTD214 airways found inside KLTSD414 packages. The KLTSD414 airway has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectible Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Glass defect located on the interior neck of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candy Sweet Spots Recalled by Bee International, Inc. Due to Undeclared Egg
The Issue: Bee International is recalling Sweet Spots Candy because it has undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: Sterility of medical devices intended for use in surgical procedures may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.