Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,588 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,588 in last 12 months

Showing 61616180 of 27,833 recalls

Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 1.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible out...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Ag Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Ag Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: Revize Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: Revize-X Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend MP Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 4.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 2.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: TissueMend Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend PRS Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis CII Safe Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinet devices plugged into any multi-socket outlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-10 Recalled by...

The Issue: There are potential risks of the Hemospray powder adhering to the distal end...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-7 Recalled by...

The Issue: There are potential risks of the Hemospray powder adhering to the distal end...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Olympus Corporation of the Americas

Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...

The Issue: Dilator tips may break in the package and in patients during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended...

The Issue: Identified a decreased performance reliability rate, Run abortions could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (V1 and V2 Recalled by Qiagen GmbH...

The Issue: Identified a decreased performance reliability rate, Run abortions could...

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

Class II — Potential Health HazardOngoing