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. 2,489 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,489 in last 12 months

Showing 2470124720 of 52,120 recalls

Medical DeviceOctober 22, 2018· Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Essence Multi-slice CT Scanner System Product Usage: The Recalled...

The Issue: Software defect: For Helical scan with ClearView function, when small arc...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice...

The Issue: Software defect: For Helical scan with ClearView function, when small arc...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Bullet Tip...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard Knee System -PS Open Box Femoral Left Recalled by Zimmer Biomet,...

The Issue: Label on the outer carton or the patient labels does not match label on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail¿ System - Tear Drop Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Becton Dickinson & Co.

Recalled Item: BD BBL Trypticase Soy Agar with 5% Sheep Blood Recalled by Becton Dickinson...

The Issue: a portion of a single lot was not manufactured in accordance with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· bioMerieux, Inc.

Recalled Item: VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more...

The Issue: False resistant results for Streptococcus anginosus and Streptococcus...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Smooth Guide Wire - Bullet Tip Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS zee biplane systems with Material 10094141- a Angiographic x-ray...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q biplane with Material 10848282- - a Angiographic x-ray Recalled by...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q.zen biplane with Material 10848355 - a Angiographic x-ray Recalled...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
DrugOctober 19, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Phenylephrine 25 mg added to NS 250 mL Bag Recalled by Avella of Deer...

The Issue: Lack of assurance of sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Hydromorphone (0.2 mg/mL) in NS 100 mL Bag Recalled by Avella of Deer...

The Issue: Lack of assurance of sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2018· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: children's allergy (cetirizine hydrochloride) Oral Solution Recalled by Taro...

The Issue: Failed Impurities/Degradation Specifications: unknown impurity higher than...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2018· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: children's allergy relief (cetirizine hydrochloride) oral solution Recalled...

The Issue: Failed Impurities/Degradation Specifications: unknown impurity higher than...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund