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 3341–3360 of 30,923 recalls
Recalled Item: Soltive Premium SuperPulsed Laser - Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser Systems-Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSDuet Premium Sample Preparation System Recalled by Becton, Dickinson...
The Issue: Sample preparation system with software may cause: 1) Multidispense feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Procedure Kit Recalled by Merit Medical Systems, Inc. Due to 7F...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Sheath Introducer 7.5F Recalled by Merit Medical Systems, Inc. Due...
The Issue: 7F sheath introducers labeled as 7.5F
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Seer Home System is an ambulatory electroencephalograph (EEG) system...
The Issue: During CAPA investigations of sight production inconsistencies, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (narrow indication)-Intended for...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation...
The Issue: Product packaging process may result in an improper or incomplete seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vios Monitoring System Bedside Monitor Model BSM2050 Recalled by Murata...
The Issue: Batteries may deplete over time while not in use if devices are stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILIZABLE INTERNAL DEFIBRILLATION PADDLES STERILIZABLE INTERNAL...
The Issue: Due to customer complaints and out of box failures, the firm is conducting a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion Pro 24 Recalled by Epilog Laser Corp. Due to a. A small number of...
The Issue: a. A small number of Fusion Pro 24 units were released with an incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAILIES TOTAL1 Recalled by Alcon Research LLC Due to Material with a quality...
The Issue: Material with a quality issue was used in contact lens production, so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewPoint 6 Recalled by GE Healthcare GmbH Due to The National Institute of...
The Issue: The National Institute of Standards and Technology (NIST) has identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual...
The Issue: Potential for product leakage from the Spin Lock Connector on the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewPoint Recalled by GE Healthcare GmbH Due to The National Institute of...
The Issue: The National Institute of Standards and Technology (NIST) has identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Option Taper Sleeve Recalled by Zimmer GmbH Due to Mislabeling
The Issue: Mislabeled: Incorrect sleeve in the packaging. The outer packaging is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or Recalled...
The Issue: Machines equipped with BPM3 Blood Pressure Modules (Blood pressure monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Option Taper Sleeve Recalled by Zimmer GmbH Due to Mislabeling
The Issue: Mislabeled: Incorrect sleeve in the packaging. The outer packaging is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional...
The Issue: A half-threaded bolt was included in the LTE kits instead of the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO Integrated Cutting System (MICS) HANDPIECE Recalled by Howmedica...
The Issue: Stryker has identified an issue with the characterization process that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.