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. 2,540 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,540 in last 12 months

Showing 1772117740 of 49,677 recalls

Medical DeviceAugust 14, 2020· Zimmer Biomet, Inc.

Recalled Item: Dual Mobility Vivacit-E Bearing Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The outer package is labeled as a Size C 38 mm, however, the implant inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...

The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Clinical Innovations, LLC

Recalled Item: Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture Recalled...

The Issue: Possible false negative or false positive results. The incorrect sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Battelle Memorial Institute

Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...

The Issue: Masks processed at one site were not maintained at levels of condensation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Sobel Westex

Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...

The Issue: Due to non-surgical isolation gowns not meeting all performance test...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Pharmaceutical Innovations, Inc.

Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...

The Issue: The firm registered the product as a Class I device, but has since been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...

The Issue: Connector between support surface and pump may be out of tolerance resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrogenase L-P Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
DrugAugust 10, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Aurobindo Pharma USA...

The Issue: Presence of Foreign Substance: product complaints were received by the firm...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2020· Sanofi-Aventis U.S. LLC

Recalled Item: Elitek (rasburicase) for injection Recalled by Sanofi-Aventis U.S. LLC Due...

The Issue: Failed Stability Specifications: Out of Specification result for enzyme...

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

Class II — Potential Health HazardOngoing
Refund