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. 3,026 recalls have been distributed to California in the last 12 months.
Showing 8881–8900 of 56,506 recalls
Recalled Item: Digoxin Tablets Recalled by Marlex Pharmaceuticals, Inc. Due to Labeling:...
The Issue: Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Digoxin Tablets Recalled by Marlex Pharmaceuticals, Inc. Due to Labeling:...
The Issue: Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Detector H. Pylori Recalled by Immunostics, Inc. Due to Labeling for...
The Issue: Labeling for affected lots incorrectly indicates the expiration date is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...
The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60/V60 Plus Ventilator Recalled by Philips Respironics,...
The Issue: Power Management PCBAs may malfunction, causing a power failure leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doxil (doxorubicin hydrochloride liposome injection) 50 mg in 25 mL (2...
The Issue: CGMP Deviations: Product was exposed to temperatures exceeding the labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...
The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Medical Products stored on pallets Recalled by Inmar Supply Chain...
The Issue: Various medical devices potentially exposed to rodent and rodent activity....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Full screen error message may occur on patient monitors with affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Contract...
The Issue: Defective Container: slow leakage under the cap
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinchlock SS Knotless Anchor Inserter Recalled by Stryker Corporation Due to...
The Issue: Expired Product distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Portex Bivona Pediatric Tracheostomy Tube Recalled by Smiths...
The Issue: The unit box is labeled with an incorrect expiration date (the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Knee insert...
The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...
The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apellis Injection Kit 29g Injection Needle -single use intended to Recalled...
The Issue: 19-gauge x 1" inch filter needles showed appearances of a small fraction of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett Cuff Pressure Manager Recalled by Covidien Due to Inadequate...
The Issue: Inadequate internal fixation of the power inlet port to the cuff pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used Recalled...
The Issue: Handbook Revision (Rev13) a dilution step is indicated as an Action when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm...
The Issue: Some catheter kits labeled as 23 cm implant length incorrectly included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.