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 29721–29740 of 56,506 recalls
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by GETINGE US SALES LLC Due to The...
The Issue: The manufacturer received complaints indicating that the device's central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Recalled...
The Issue: Device may display a battery missing error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Recalled by...
The Issue: RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray)...
The Issue: Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured...
The Issue: The firm was notified by the State of TN that the product contained...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MAN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.8 OZ (51g) Recalled by eBars Due...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WOMAN ORGANIC DARK CHOCOLATE BERRY bar NET WT. 1.8 OZ Recalled by eBars Due...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FOCUS FOR KIDS! SUNFLOWER SEED CHOCOLATE STRAWBERRY bar NET WT. Recalled by...
The Issue: The product test positive for peanuts and almond allergen which is not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8 Recalled by...
The Issue: The firm was notified by the State of TN that the product contained...
Recommended Action: Do not consume. Return to store for a refund or discard.