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. 2,696 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,696 in last 12 months

Showing 80818100 of 52,482 recalls

Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· B. Braun Medical, Inc.

Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...

The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2023· B. Braun Medical, Inc.

Recalled Item: 8713052U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...

The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 21, 2023· Acclarent, Inc.

Recalled Item: TruDi Navigation System Recalled by Acclarent, Inc. Due to When using...

The Issue: When using affected curette and software, there is a discrepancy between the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 20, 2023· KVK-Tech, Inc.

Recalled Item: Betaxolol Tablets Recalled by KVK-Tech, Inc. Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: There is a potential presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 20, 2023· Imprimis NJOF, LLC

Recalled Item: MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile...

The Issue: Subpotent: Out of Specification result observed for Ketorolac assay levels,...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 20, 2023· Vive Organic

Recalled Item: 2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT...

The Issue: Undeclared allergen; coconut

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack Recalled by...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject 20 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2023· Cardinal Health 200, LLC

Recalled Item: Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack Recalled by Cardinal Health...

The Issue: Demonstrated recognition and compatibility issues with syringe infusion pumps.

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

Class I — Serious Health HazardOngoing
FoodSeptember 19, 2023· HEINZ

Recalled Item: Kraft Singles American Pasteurized Prepared Cheese product Recalled by HEINZ...

The Issue: Plastic fragment. Product is recalled due to potential for a thin strip of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2023· NeuroSync, Inc.

Recalled Item: NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists...

The Issue: Eye syncing issues causing the device to be inoperable. Unable to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2023· Magellan Diagnostics, Inc.

Recalled Item: LeadCare II Blood Lead Test Kit-For in vitro diagnostic use Recalled by...

The Issue: During an internal audit a small percentage (<10%) of plastic caps used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2023· Atrium Medical Corporation

Recalled Item: Express Dry Seal Chest Drains (Express): 4000-100N DRAIN Recalled by Atrium...

The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2023· Atrium Medical Corporation

Recalled Item: Ocean Water Seal Chest Drains (Ocean): Products Product Recalled by Atrium...

The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2023· Atrium Medical Corporation

Recalled Item: Oasis Dry Suction Water Seal Chest Drains (Oasis): (1)3600-100 DRAIN...

The Issue: Instructions for Use (IFU) for the Atrium Ocean, Oasis, and Express chest...

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

Class II — Potential Health HazardOngoing