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 2536125380 of 30,923 recalls

Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: AC TenderLink 13/30 10 pcs Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: Infusion Set Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Unomedical As

Recalled Item: SureT G29 6mm Recalled by Unomedical As Due to Tubing detachment

The Issue: Tubing detachment

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: MINI PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· Synthes (USA) Products LLC

Recalled Item: Synthes Small Electric Drive (SED) Recalled by Synthes (USA) Products LLC...

The Issue: The device may operate solely in reverse mode, not operate in reverse mode...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS CHEMISTRY PRODUCTS TRIG Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Potential for biased results using the specific lot of VITROS CHEMISTRY...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: CONMED ADULT R2 Multifunction Electrodes Recalled by ConMed Corporation Due...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· Abbott Medical Optics Inc (AMO)

Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...

The Issue: AMO has received complaints where the finger grip dislodged while depressing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2014· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer Fisher and...

The Issue: Breakage of the nut that secures the heater head in place, which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2014· ConMed Corporation

Recalled Item: PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due to...

The Issue: Philips Healthcare made changes to the design of the connection between...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 5, 2014· Philips Ultrasound, Inc.

Recalled Item: Q-Station Quantification Software. Q-Station 3.0 with a2DQ and/or aCMQ...

The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2014· Toshiba American Medical Systems Inc

Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...

The Issue: Potential problem with the cardiac function analysis software (CFA)....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2014· Philips Ultrasound, Inc.

Recalled Item: EPIQ 5 Ultrasound System Recalled by Philips Ultrasound, Inc. Due to When...

The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2014· Philips Ultrasound, Inc.

Recalled Item: Additional devices identified in new FSN MA-FCO 83000190: QLAB versions...

The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...

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

Class II — Potential Health HazardOngoing