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. 2,856 recalls have been distributed to California in the last 12 months.
Showing 22841–22860 of 56,506 recalls
Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...
The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...
The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TAINY VOSTOKA ASSORTED DRIED FRUITS -APPLE were distributed nationwide in...
The Issue: Product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TAINY VOSTOKA ASSORTED DRIED FRUITS - QUINCE packaged in 500gram (17.65oz)...
The Issue: Product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...
The Issue: Reports have been received of the CentriMag Systems experiencing motor and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concerto & Basic Shower Trolly Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....
The Issue: The firm has become aware that any of the 4 safety catches may exhibit a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Recalled by LivaNova USA Inc Due to Sentiva generators may reset...
The Issue: Sentiva generators may reset and become disabled within 60 days of enabling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System Recalled...
The Issue: Potential need for device replacement - Elective Replacement Indicator (ERI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GUIDE WIRE 2.2MM X 28IN Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive HHR Tess Cleat Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0MM BALL NOSE GUIDE WIRE Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Copeland HA Resurfacing Head Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Recalled by Zimmer Biomet, Inc. Due to Elevated levels of bacterial...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500...
The Issue: Incorrect labeling on the products package. The label on the package shows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioEnvelope Recalled by AZIYO BIOLOGICS Due to Possible suture brittleness...
The Issue: Possible suture brittleness or breakage along the Envelope seam before the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Custom Products Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENNESSY LEFT CONST GLENOID HA Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LT DISC ULNA - HA/PC Recalled by Zimmer Biomet, Inc. Due to Elevated levels...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Recalled by...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive RS Cleat CAP Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.