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 45981–46000 of 56,506 recalls
Recalled Item: CooperSurgical MILEX PESSARY KITS-Ring w/Support Folding Pessary- #1 Model:...
The Issue: Incorrect expiration date printed on the MILEX PESSARY KIT packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...
The Issue: Packaging of a device was compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DOPamine Hydrochloride and 5% Dextrose INJ Recalled by Baxter Healthcare...
The Issue: Lack of Assurance of Sterility: A small cut in the solution bag may have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ASTS-LG1212: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic...
The Issue: Product is mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Selector Kit Sterile single use device A bi-lumen Recalled by...
The Issue: Some specific lots of Selector Tubing may potentially leak irrigation fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dharma Cavity Varnish 15mL Recalled by Dharma Research, Inc. Due to During...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dharma Cavity Varnish with Fluoride Recalled by Dharma Research, Inc. Due to...
The Issue: During an FDA inspection, it was found that the products are being marketed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....
The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...
The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...
The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Presence of split or broken tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Sun Pharma...
The Issue: Failed Dissolution Specifications; 12 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specification; at the 6-month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pilling Knife Handles: a) b) c) Recalled by Teleflex Medical Due to The...
The Issue: The knife handles slot depth is out of specification, so blades may not fit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Saturated Gauze Dressing Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Post-op Surgical Kits Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Wound Dressing Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Daily Dressing Packets Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Calibrator E Recalled by Siemens Healthcare Diagnostics, Inc Due to...
The Issue: Positive bias for Calibrator E lot kits ending in 38 and 39 with the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...
The Issue: These microcatheters were packaged with a 2.8 F distal tip, rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.