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.

56,506 total recalls
2,839 in last 12 months

Showing 2504125060 of 30,923 recalls

Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)IR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerator: ARTISTE Recalled by Siemens Medical Solutions...

The Issue: Use of any unauthorized third-party components on Siemens LINACs may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2014· Stelkast Co

Recalled Item: EXp Tibial Insert Recalled by Stelkast Co Due to Difficulty locking EXp...

The Issue: Difficulty locking EXp tibial inserts into tibial trays, caused by a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult AirLife dual-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife single-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife Dual- Recalled by Vyaire Medical Due to Manufacturing error...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number:...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 26, 2014· Lacrimedics Inc

Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...

The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2014· Getinge Disinfection Ab

Recalled Item: GETINGE 46-SERIES Medical Washer-Disinfector Recalled by Getinge...

The Issue: Getinge Disinfection AB received complaints regarding sediment residuals in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2014· SCC Soft Computer

Recalled Item: SoftPath Laboratory Information System. Versions 4.3.0.8 Recalled by SCC...

The Issue: Modifications to diagnostic text may be: 1) Saved to the database but not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2014· St Jude Medical

Recalled Item: TactiSys Quartz Pack Recalled by St Jude Medical Due to A configuration...

The Issue: A configuration update needs to be done on TactiSys to appropriately...

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

Class II — Potential Health HazardOngoing