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. 2,623 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,623 in last 12 months

Showing 1012110140 of 28,579 recalls

Medical DeviceFebruary 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Interventional Fluoroscopic X-Ray System - Product Usage: developed for...

The Issue: Siemens has become aware of a potential issue in which the imaging system...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· CAIRE DIAGNOSTICS INC

Recalled Item: CAIRE DIAGNOSTICS FenomPro SN ***** - Product Usage: a portable Recalled by...

The Issue: Erroneously high FeNO levels which may contribute to premature...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2021· Accuray Incorporated

Recalled Item: CyberKnife Treatment Delivery System - Product Usage: indicated for...

The Issue: The set screws that connect the Standard Treatment Couch linkage arm to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit - Product Usage: intended for use in Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus MNC Apheresis Kit - Double Needle - Product Usage: Recalled by Fenwal...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Fenwal Inc

Recalled Item: Amicus Exchange Kit Therapeutics - Product Usage: intended for use Recalled...

The Issue: Some lots of Amicus MNC Apheresis and Amicus Exchange kits have leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Sterile Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Bulk Non-Sterile Recalled by Cardinal Health 200,...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: Femoral Angiography Drape Sterile Recalled by Cardinal Health 200, LLC Due...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2021· Cardinal Health 200, LLC

Recalled Item: In-View Clear Leggings Bulk Non-Sterile Recalled by Cardinal Health 200, LLC...

The Issue: Cardinal Health has determined that a manufacturing variance in a plastic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Arthrex, Inc.

Recalled Item: Drill Bit Recalled by Arthrex, Inc. Due to The color indicator on the...

The Issue: The color indicator on the proximal end of the shaft of the AR-8770-02 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Philips CT systems are advanced continuous-rotation computed tomography...

The Issue: Philips has internally detected an issue with the actuators used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2021· Trinity Sterile, Inc.

Recalled Item: Midline Catheter Dressing Change Kit with Statlock - Product Usage: Recalled...

The Issue: Evidence of face masks or other material in the seal in several kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to For some LINAC...

The Issue: For some LINAC types, merging clinical beams with beams of approximate dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI Recalled by...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing