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. 1,074 recalls have been distributed to California in the last 12 months.
Showing 35321–35340 of 56,506 recalls
Recalled Item: Neeras Spicy Thai Sauce and Marinade Recalled by Cinnabar Specialty Foods,...
The Issue: Product contains undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Olanzapine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: due to out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Succinylcholine Chloride Recalled by Pharmedium Services, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: A portion of the batch quantity was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ben & Jerrys Brownie Batter Core Ice Cream One Pint Recalled by Unilever...
The Issue: Certain pints of Ben & Jerrys Brownie Batter Core Ice Cream may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW...
The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING...
The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Force Nephrostomy Balloon Dilation Catheter Kit with Inflation Device...
The Issue: Contract manufacturer packaged an incorrect sheath with the product....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING...
The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED OVERSIZED...
The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING...
The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED SELF-TAPPING...
The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...
The Issue: Encoded with incorrect ranges that are not consistent with the ranges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...
The Issue: Potential presence of particulate matter on the blood side of the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...
The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING...
The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF MultiGen¿ Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker Instruments is voluntarily recalling the Care...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay Recalled by...
The Issue: Abbott has identified negative interference from the drug N-Acetyl Cysteine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain Recalled by Zimmer Biomet, Inc. Due to Complaint of the head...
The Issue: Complaint of the head holder connector locking up mechanically when tightened.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System Product Usage: RayStation is a...
The Issue: An error may occur with the display of dose computed on images other than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Algovita Spinal Cord Stimulation System Recalled by Nuvectra Due to Nuvectra...
The Issue: Nuvectra is conducting a recall due to two clinical risks that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.