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 2718127200 of 30,923 recalls

Medical DeviceDecember 16, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Covidien

Recalled Item: Puritan Bennett 840 ventilator systems software part number 4-070212-85...

The Issue: Covidien is conducting a voluntary field corrective action on Puritan...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2013· Highland Metals, Inc.

Recalled Item: SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 Recalled...

The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2013· Highland Metals, Inc.

Recalled Item: SuperElastic Regular force NiTi lower or upper Natural arches. 0.14 Recalled...

The Issue: Labeling issue: Product labeled as "Upper" may contain "Lower" archwires...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2013· King Systems Corp.

Recalled Item: King Systems KLTSD414 Quantity Recalled by King Systems Corp. Due to KLTD214...

The Issue: KLTD214 airways found inside KLTSD414 packages. The KLTSD414 airway has a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: CODMAN CERTAS Programmable Valves Recalled by Codman & Shurtleff, Inc. Due...

The Issue: Ensuring all customers have the tools to assist in verifying the setting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: Sterility of medical devices intended for use in surgical procedures may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· King Systems Corp.

Recalled Item: King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled...

The Issue: On December 13, 2012, King Systems initiated a voluntary recall of one (1)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2013· GE Healthcare

Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...

The Issue: Medical device adjustment knob may be loose and affect the accuracy of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· AdvanDx, Inc.

Recalled Item: AdvanDx Gram-Negative QuickFISH BC. In-Vitro Diagnostic for the...

The Issue: Kits incompatible with certain fluorescence microscope light sources

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

Class III — Low RiskOngoing
Medical DeviceDecember 11, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2013· Toshiba American Medical Systems Inc

Recalled Item: TSX-301C Aquilion One (Vision Edition) Computed Tomography X-Ray System....

The Issue: Toshiba America Medical Systems, Inc. initiated this recall due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Zimmer, Inc.

Recalled Item: Versys Build-Up Block The VerSys CRC Hip System is indicated Recalled by...

The Issue: Zimmer is initiating a lot specific recall of the CPT Hip Stem, Versys...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2013· Draeger Medical Systems, Inc.

Recalled Item: Draeger Infinity Acute Care System Monitoring Solution Recalled by Draeger...

The Issue: After a test in which a low SpO2 (yellow) medium grade alarm initiated in...

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

Class II — Potential Health HazardOngoing