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. 2,839 recalls have been distributed to California in the last 12 months.
Showing 25521–25540 of 30,923 recalls
Recalled Item: Accusorb MRI MAC7005 Part Number: MRI-05 Leg Wrap Product Usage: Recalled by...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7001 Part Number: MRI-01 MRI-Large Blanket Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7003 Part Number: MRI-03 U (Upper) and MRI-03 Recalled by...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7010 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alliance Tech Medical Recalled by Alliance Tech Medical, Inc Due to Patients...
The Issue: Patients have experienced a bad taste associated with the filters.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...
The Issue: This strain should be resistant to high levels of Gentamicin and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...
The Issue: This strain should be resistant to high levels of Gentamicin and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to This strain should be...
The Issue: This strain should be resistant to high levels of Gentamicin and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FullFire Diffusing Tip Laser Probe Recalled by Monteris Medical Corp Due to...
The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...
The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SideFire Directional Laser Probe Recalled by Monteris Medical Corp Due to...
The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...
The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...
The Issue: Failed to meet established requirements for sterile barrier integrity due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...
The Issue: The affected products are missing polar boss threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...
The Issue: A software issue may lead to ventilator inoperative situations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS Operating Room table (ORT200 and ORT300). Intended for use Recalled by...
The Issue: One of the three pins that is used to hold the ORT200 table alignment block...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...
The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...
The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...
The Issue: The caster may separate completely from the device frame causing injury to user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.