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. 3,022 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,022 in last 12 months

Showing 99019920 of 30,923 recalls

Medical DeviceJune 23, 2021· Covidien Llc

Recalled Item: Covidien Sonicision Reusable Generator-converts electrical power from the...

The Issue: Potential for a manufacturing assembly error-may result in a non-functional...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2021· BioMerieux SA

Recalled Item: MYLA software. Used to manage microbiology test workflow from the Recalled...

The Issue: Software anomaly - Under certain conditions, unwanted alterations to results...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Murata Vios, Inc.

Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...

The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Accora Inc

Recalled Item: Configura Advance Chair Recalled by Accora Inc Due to The firm has...

The Issue: The firm has identified a potential for the backrest to become detached from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA Self Safe Recalled by Delta Med SpA Due to Problems related to the...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA Self Safe 1 Recalled by Delta Med SpA Due to Problems related to...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA Self Safe T Recalled by Delta Med SpA Due to Problems related to...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed Recalled by Delta Med...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) Recalled by...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN FASTFLASH Recalled by Delta Med SpA Due to Problems related to the...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR 1 Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...

The Issue: Problems related to the sterilization of the medical devices; possible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2021· WOM World of Medicine AG

Recalled Item: Covidien HysteroLux Fluid Management System Control Unit Recalled by WOM...

The Issue: When the display of inflow volume to the uterus reaches 32450 ml, the fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2021· Remel Inc

Recalled Item: ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in...

The Issue: Out of Specification

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2021· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and...

The Issue: It has been identified that ventilators equipped with High Flow Therapy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 18, 2021· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10....

The Issue: It has been identified that ventilators equipped with High Flow Therapy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2021· Gentherm Medical, LLC

Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Gentherm Medical, LLC...

The Issue: There is a potential risk of device contamination and patient infection...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing