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. 2,595 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,595 in last 12 months

Showing 1272112740 of 28,579 recalls

Medical DeviceNovember 6, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Color Cuff Disposable Tourniquet Cuff Recalled by Stryker Instruments Div....

The Issue: There is a potential for the cuff to leak air leading to a loss of vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2019· Allergan PLC

Recalled Item: Natrelle Silicone Filled Breast Implants for the following Styles and...

The Issue: The firm has became aware that 2D barcodes on breast implants and sizers may...

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2019· Qualigen Inc

Recalled Item: The FastPack System Comlete Immunoassay Kit Immunoassay for the Quantitative...

The Issue: The chemiluminescent immunoassay has been noted to have higher than expected...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Dako Denmark A/S

Recalled Item: Dako Autostainer instruments: Autostainer Link 48 Recalled by Dako Denmark...

The Issue: The Autostainer instrument may not have a syringe tray installed which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· King Systems Corp. dba Ambu, Inc.

Recalled Item: King Vision Video Adapter Size 1/2. Laryngoscope used to examine Recalled by...

The Issue: Exhibiting a reversed image. Although the image may appear normal, the users...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 5, 2019· Avanos Medical, Inc.

Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...

The Issue: Avanos Medical has received reports stating that the central lumen of some 5...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Integra Lifesciences Sales Llc

Recalled Item: Ascension¿ Silicone PIP-Silicone PIP Sz 1 Recalled by Integra Lifesciences...

The Issue: Silicone PIP Implant mislabeled as a size 1 implant on the outer packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Medacta Usa Inc

Recalled Item: Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS Recalled by Medacta...

The Issue: Certain lot numbers of the Medacta Humeral Anatomical Cementless Metaphysis...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Becton Dickinson & Company

Recalled Item: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of...

The Issue: The indicator may show available charge when the battery is close to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Shimadzu Medical Systems

Recalled Item: Trinias DAP Meter Recalled by Shimadzu Medical Systems Due to The DAP meters...

The Issue: The DAP meters were found to be outside of tolerance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to the...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Trilliant Surgical, LLC

Recalled Item: 8mm HTR Sterile Hammer Toe Reaming Kit Recalled by Trilliant Surgical, LLC...

The Issue: The firm has identified that parts from the kit, lot: TSL007202, have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing