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. 2,646 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,646 in last 12 months

Showing 46814700 of 49,677 recalls

Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - For implantation to reinforce...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.7-2 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Paracentesis Thoracente Recalled by American Contract Systems, Inc. Due to...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Cath Lab Pack Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Fisher & Paykel Healthcare, Ltd.

Recalled Item: PT301US Airvo 3 Respiratory Support Device with software version 1.2.0...

The Issue: Due to a software issue, affected devices that are set up with High Pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Endovascular AAA Pack Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Shoulder Recalled by American Contract Systems, Inc. Due to ACS identified...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.7 - For implantation to reinforce...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.4-2 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Cysto Recalled by American Contract Systems, Inc. Due to ACS identified that...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.2 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPB-0.4 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Essentia MAJ Laparotomy Std Pack Recalled by American Contract Systems, Inc....

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Day Surgery General Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.2-2 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.4 - For implantation to reinforce...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: ENT Recalled by American Contract Systems, Inc. Due to ACS identified that...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Arthroscopy Pack Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Open Shoulder Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing