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 1601–1620 of 30,923 recalls
Recalled Item: Model Number SM-40HF-B-D-C Recalled by SEDECAL SA Due to Sedecal sent an...
The Issue: Sedecal sent an email to its consignees to remind the users that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...
The Issue: Select orders of lenses were manufactured with errors impacting sagittal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...
The Issue: Select orders of lenses were manufactured with errors impacting sagittal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CHE Slides Recalled by Ortho-Clinical Diagnostics,...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross Access Solution (VXSK) Recalled by Boston Scientific Corporation...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...
The Issue: As a result of a comprehensive product performance review it was determine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Akreos Recalled by Bausch & Lomb Surgical, Inc. Due to An off-power error...
The Issue: An off-power error was identified, which resulted in a diopter of 16, rather...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Manifold Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tubing Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Pressure Tubing: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Waste Management Kit: Recalled by Merit Medical Systems, Inc. Due to...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zvu Anorectal Manometry Procedure Kit Recalled by Diversatek Healthcare Due...
The Issue: Anorectal manometry procedure kit outer kit label is mislabeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.