Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,098 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,098 in last 12 months

Showing 15261–15280 of 52,482 recalls

FoodAugust 13, 2021· Kansas City LLC., DBA Best Harvest Bakeries

Recalled Item: Hotdog buns Recalled by Kansas City LLC., DBA Best Harvest Bakeries Due to...

The Issue: Positive environmental samples analyzed for Listeria and Salmonella species.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 13, 2021· Hostess Brands, LLC

Recalled Item: Hostess Soft White Hamburger Buns Recalled by Hostess Brands, LLC Due to...

The Issue: The firm's contract manufacturer found positive environmental samples...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· SigmaPharm Laboratories LLC

Recalled Item: Sodium Phenylbutyrate POWDER Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Failed Impurities Specifications: Out of Specification impurity results...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg/1mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Akorn, Inc.

Recalled Item: Betamethasone Dipropionate Lotion USP (Augmented) Recalled by Akorn, Inc....

The Issue: Failed impurities/degradation specification: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2021· AMTEC SALES Inc

Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...

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 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Elition X-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel Recalled by Red...

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 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: OctoStretch with Stretch Leveller - The combination of this products...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: FlexoStretch Model Number: 3156057 - The combination of this products...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition S-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing