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. 1,853 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,853 in last 12 months

Showing 3986139880 of 52,482 recalls

DrugMay 4, 2015· Ohm Laboratories, Inc.

Recalled Item: Loratadine Orally Disintegrating Tablets USP Recalled by Ohm Laboratories,...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
FoodMay 4, 2015· Natural Creations Inc

Recalled Item: Natural Creations Glucosamine MSM 90 capsules packaged in 250 cc Recalled by...

The Issue: Natural Creations is recalling Glucosamine MSM dietary supplement due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 4, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to The heart rate could be...

The Issue: The heart rate could be calculated from pacer pulses without indication that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2015· Spine Wave, Inc.

Recalled Item: Spine Wave Access Kit Recalled by Spine Wave, Inc. Due to Mislabeling

The Issue: Mislabeled outer carton: Monopolar Probe is listed as 200 x 1.5mm when it...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Navigation System II-Cart Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker initiated a device recall of the Navigation System II-Cart, Camera...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2015· Smiths Medical Asd Inc

Recalled Item: Low Volume Extension Set Recalled by Smiths Medical Asd Inc Due to Smiths...

The Issue: Smiths Medical has become aware of an issue with the Low Volume Extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2015· Remel Inc

Recalled Item: Remel Blood Agar (TSA w/sheep blood) plate packaged Recalled by Remel Inc...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2015· Synovis Surgical Innovations, Inc.

Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...

The Issue: Baxter healthcare is recalling specific product codes of Vascu-Guard...

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

Class I — Serious Health HazardOngoing
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Sun Rich Apple Slices with Caramel Dip Recalled by Sun Rich Fresh Foods Inc...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Sunshine Salad Kit Recalled by Sun Rich Fresh Foods Inc Due to Potential...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Fresh Cut Red Apple Slices 2 x 3 lbs Recalled by Sun Rich Fresh Foods Inc...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Sub Way Apple Slices Recalled by Sun Rich Fresh Foods Inc Due to Potential...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2015· Sun Rich Fresh Foods Inc

Recalled Item: Fresh Cut Mixed Apple slices Recalled by Sun Rich Fresh Foods Inc Due to...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 1, 2015· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...

The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Biomet, Inc.

Recalled Item: Unilateral external fixation ankle clamp Product Usage: Unilateral external...

The Issue: Ankle clamp was assembled incorrectly; the offset of the pin to the pivot...

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

Class II — Potential Health HazardOngoing