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 2586125880 of 30,923 recalls

Medical DeviceJuly 17, 2014· Zimmer, Inc.

Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Cook Inc.

Recalled Item: CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a...

The Issue: This remedial action is the result of six product complaints associated with...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Vital Sync RMS 1.0 when loaded with v2.4 software Recalled by Nellcor...

The Issue: Covidien is conducting a field correction of the Vital Sync Virtual Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Vital Sync" VPMP & IM Recalled by Nellcor Puritan Bennett Inc. (dba Covidien...

The Issue: Covidien is conducting a field correction of the Vital Sync Virtual Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs...

The Issue: Customers may receive positively biased results when using VITROS¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· AGFA Healthcare Corp.

Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some sheets...

The Issue: Some sheets of the medical screen film are fogged.

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

Class III — Low RiskOngoing
Medical DeviceJuly 16, 2014· Market-Tiers Inc

Recalled Item: Instructions for Use for the blue endo MOREsolution Electromechanical...

The Issue: Some pages of the Instructions for Use were omitted, including pages...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension EXL Integrated Chemistry System in vitro diagnostic...

The Issue: The Reagent Lid hinge may lose its effectiveness and slowly shift downward...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Chemistry Wash (RD701) is an accessory of the Recalled by...

The Issue: Siemens Healthcare Diagnostics has received complaints for the Dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2014· Vascutek, Ltd.

Recalled Item: Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a Recalled...

The Issue: The cautery that is provided with the Gelweave graft in the box has a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2014· Baxter Healthcare Corp

Recalled Item: ***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m) Recalled by Baxter...

The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: Tibila Insert UC Recalled by Ortho Development Corporation Due to Ortho...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Baxter Healthcare Corporation

Recalled Item: FlowCOUPLER. An implantable device that is used to detect blood Recalled by...

The Issue: Baxter Healthcare is recalling the FlowCOUPLER Device because there is a...

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

Class II — Potential Health HazardOngoing