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. 3,068 recalls have been distributed to California in the last 12 months.
Showing 2961–2980 of 56,506 recalls
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....
The Issue: Incorrect blister labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...
The Issue: It was determined that the consumable issue may result in No Call - INT CTL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....
The Issue: software issue that causes an error screen on a portable vital signs monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bone & Joint Restore. 180 capsules in a plastic bottle. Recalled by Optimal...
The Issue: Potential for contamination with salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dexonto 0.4% (dexamethasone sodium phosphate) solution 20 mg/5 mL (4 mg/mL)...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date: Individual vials...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL) Recalled by OurPharma LLC Due...
The Issue: Superpotent Drug: Assay/potency result for hydromorphone HCl in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number:...
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376....
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient Monitor software update to address issues:1)May freeze at startup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: La Victoria Cilantro Salsa Recalled by MegaMex Foods LLC Due to Foreign...
The Issue: Firm's salsa product was potentially manufactured with a recalled ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELECTRO BUZZ Recalled by SAINI TRADE INC Due to Undeclared Chloropretadalafil
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA ARMOR Recalled by SAINI TRADE INC Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Male Ultra Pro Recalled by SAINI TRADE INC Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MALEXTRA Recalled by SAINI TRADE INC Due to Undeclared Propoxyphenylsildenafil
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.