Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,677 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,677 in last 12 months

Showing 36813700 of 29,186 recalls

Medical DeviceJune 20, 2024· Securitas Healthcare LLC

Recalled Item: Arial Call Station Recalled by Securitas Healthcare LLC Due to This is a...

The Issue: This is a risk that alarms will not be received by the Arial Wireless Nurse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...

The Issue: If blood culture identification panel is used in conjunction with specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Foundation Medicine, Inc.

Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...

The Issue: Two (2) reports were sent to customers with an incorrect negative claim on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Angiodynamics, Inc.

Recalled Item: SOFT-VU KUMPE 5F X 40CM -Used for patients in need Recalled by...

The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Angiodynamics, Inc.

Recalled Item: SOFT-VU KUMPE 5F X 65CM -Used for patients in need Recalled by...

The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Embecta Corp.

Recalled Item: BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count Recalled by Embecta Corp. Due...

The Issue: BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· Medtronic Neuromodulation

Recalled Item: Medtronic Handset with Communicator Recalled by Medtronic Neuromodulation...

The Issue: A subset of the handsets within the kit may not be able to complete the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· Abbott Diagnostics Technologies AS

Recalled Item: Afinion 2 Analyzer Recalled by Abbott Diagnostics Technologies AS Due to...

The Issue: Five Afinion 2 (AF2) Analyzer were incorrectly market configured as Moderate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· ROi CPS LLC

Recalled Item: Regard Kit containing the Microtek decanter Recalled by ROi CPS LLC Due to...

The Issue: Decanters may have pin holes and tears in sterile packaging that cannot be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-Used with an Recalled by B. Braun...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DROP PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat 60DROP METRISET PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 60 DROP PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DR PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat SPACE PUMP IV SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DROP PUMP SET W/3 SAFELINE Recalled by B. Braun Medical,...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat SPACE PUMP IV SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing