Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,375 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,375 in last 12 months

Showing 4332143340 of 49,677 recalls

Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Perrigo Diabetes Care

Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...

The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...

The Issue: There is a potential for communication loss associated with the F5-01 Frame...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Zeiss, Carl Inc

Recalled Item: Compensator Slider Lambda 6x20 component (part number 473704-0000-000)...

The Issue: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Optimedica Corporation

Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...

The Issue: Potential for unexpected heating of the transformer mounting bolt located...

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

Class II — Potential Health HazardOngoing
DrugDecember 19, 2013· Abrams Royal Pharamacy

Recalled Item: MINERAL IV Injection Recalled by Abrams Royal Pharamacy Due to...

The Issue: Non-Sterility; analytical results found product to contain Sphingomonas...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 19, 2013· Abrams Royal Pharamacy

Recalled Item: All Unexpired Sterile Drug Products Recalled by Abrams Royal Pharamacy Due...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...

The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Steris Corporation

Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that the outer shipping package for one lot (Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...

The Issue: Three problems were reported to the firm: When positioning for a relative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· ITC-Nexus Dx

Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...

The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Spacelabs Healthcare, Llc

Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...

The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Biomet, Inc.

Recalled Item: Locking Cortical Screw 3.5mmX38mm Recalled by Biomet, Inc. Due to 3.5mmx38mm...

The Issue: 3.5mmx38mm Locking Cortical Screw, implants are being recalled since an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
DrugDecember 18, 2013· Teva Pharmaceuticals USA

Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2013· Teva Pharmaceuticals USA

Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund