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. 2,881 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,881 in last 12 months

Showing 2028120300 of 30,923 recalls

Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Baxter Healthcare Corporation

Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 1, 2017· BioMerieux SA

Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...

The Issue: Potential performance issue on strain categorization.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 1, 2017· Seiler Instr. & Mfg. Co. Inc.

Recalled Item: Alpha Air 6 ENT Microscope Microscope examination of the human ear Recalled...

The Issue: The microscope may tip over if attachments are fully extended in one line...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...

The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Radial Head Prosthesis System Recalled by Synthes (USA) Products LLC...

The Issue: There is the possibility that the radial stem may loosen post-operatively at...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-115: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Cisco 3850 layer 3 switch Recalled by Philips Electronics North...

The Issue: May experience a loss of centralized monitoring.

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

Class II — Potential Health HazardOngoing