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. 2,666 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,666 in last 12 months

Showing 20812100 of 28,579 recalls

Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2025· Abbott Medical

Recalled Item: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...

The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Smiths Medical ASD, Inc.

Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Airway adapter does not meet specification and may break off when attaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Smiths Medical ASD, Inc.

Recalled Item: CAPNOCHECK BCI Airway Adapter Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Airway adapter does not meet specification and may break off when attaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as PACK Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as ORTHO TRAUMA CDS Recalled by MEDLINE INDUSTRIES, LP...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape. Recalled...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing