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. 2,495 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,495 in last 12 months

Showing 1980119820 of 28,579 recalls

Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Encore Medical, Lp

Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...

The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Tecan US, Inc.

Recalled Item: SUNRISE instrument. The INFINITE F50 instrument is a 96-well absorbance...

The Issue: The batteries have the potential to overheating, melt or char.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Tecan US, Inc.

Recalled Item: Hydroflex ELISA The HYDROFLEX is a plate washer for 96-well Recalled by...

The Issue: The batteries have the potential to overheating, melt or char.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Tecan US, Inc.

Recalled Item: Infinite 200 PRO The Tecan Infinite 200 PRO is a Recalled by Tecan US, Inc....

The Issue: The batteries have the potential to overheating, melt or char.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Tecan US, Inc.

Recalled Item: Tecan Infinite 200. The SUNRISE instrument is a 96-well absorbance Recalled...

The Issue: The batteries have the potential to overheating, melt or char.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Microgenics Corporation

Recalled Item: DRI Salicylate Serum Tox Assay Recalled by Microgenics Corporation Due to...

The Issue: Some lots of DRI Salicylate Serum Tox Assay negative patient samples are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled...

The Issue: Terumo Custom Cardiovascular Procedure Kits are labeled as Xcoating surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Tecan US, Inc.

Recalled Item: Tecan Infinite M1000 PRO The Tecan Infinite M1000 PRO is Recalled by Tecan...

The Issue: The batteries have the potential to overheating, melt or char.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Tecan US, Inc.

Recalled Item: Infinite F50 instrument. The INFINITE F50 instrument is a 96-well Recalled...

The Issue: The batteries have the potential to overheating, melt or char.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Tecan US, Inc.

Recalled Item: Tecan Infinite M1000 The Tecan Infinite M1000 is a multifunctional Recalled...

The Issue: The batteries have the potential to overheating, melt or char.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to A firmware...

The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800 Recalled by GE OEC Medical Systems, Inc Due to A firmware issue in...

The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Smith & Nephew, Inc.

Recalled Item: RENASYS Sterile Transparent Film and all the RENASYS Dressing kits Recalled...

The Issue: Sterility seal integrity failures on the Renasys Sterile Transparent Film

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Inovo, Inc

Recalled Item: INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen Recalled by...

The Issue: Device can fail during operation.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Integra LifeSciences Corp.

Recalled Item: Large QWIX Compression screw Recalled by Integra LifeSciences Corp. Due to...

The Issue: Labeling on the Qwix Screw product states that it is a "compression screw"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography...

The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...

The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...

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

Class II — Potential Health HazardOngoing