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. 1,095 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,095 in last 12 months

Showing 15481–15500 of 52,120 recalls

Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A800360 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A899916 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· M.D.L. S.r.l.

Recalled Item: Soft Tissue Biopsy Needles Recalled by M.D.L. S.r.l. Due to Sterility...

The Issue: Sterility assurance may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A902616 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A319516AM Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· Beckman Coulter Inc.

Recalled Item: Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT...

The Issue: Firm's submission for Emergency Use Authorization (EUA) contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A399400A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A300316A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A902416 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A303318A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A119216M Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A300318A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A800061 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A897514 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· M.D.L. S.r.l.

Recalled Item: General Manual surgical instrument Recalled by M.D.L. S.r.l. Due to...

The Issue: Sterility assurance may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Mac Medical Supply Co Inc

Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...

The Issue: Customers have reported an increased number of false positive SARS-CoV-2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Abbott Molecular, Inc.

Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...

The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing