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. 3,072 recalls have been distributed to California in the last 12 months.
Showing 181–200 of 30,923 recalls
Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...
The Issue: The mix up of the impression caps provided in the package. The provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST100 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION Recalled by Medline...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sterile Saline Wound Wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n)...
The Issue: Potential risk of Quality Control failures and/or false resistant antibiotic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert 5R 14MM Recalled by Encore Medical, LP Due to...
The Issue: 942-01-40G acetabular system package was found to contain 942-01-36H...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer STERILE saline wound wash Recalled by Medline Industries, LP Due to...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...
The Issue: Medline has identified that the manufacturer of the sterile saline wound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raz-AT (Attendant Tilt) Mobile Shower Commode Chair Recalled by Raz Design...
The Issue: Due to a modification by a vendor and may be reinstalled without properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Acetabular System: Liner Recalled by Encore Medical, LP Due to...
The Issue: 942-01-40G acetabular system package was found to contain 942-01-36H...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...
The Issue: Due a design issue where the navigated array connection geometry is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. Recalled by AVID Medical,...
The Issue: Tyvek bag seal issue which may compromise sterility of the kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.