Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,528 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,528 in last 12 months

Showing 61216140 of 27,558 recalls

Medical DeviceMay 24, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-PRO 2- A powered ambulance cot that consists of a platform Recalled by...

The Issue: Base leg assembly may bend and result in difficulty engaging/disengaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Sterile CirClamp with 1.45cm Bell Reprocessed Recalled by MEDLINE...

The Issue: The kits incorrectly contain CirClamp subassembly 345CRSAK which results in...

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 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 PRS Meshed 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: SurgiMend 3.0 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: 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