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 73417360 of 28,744 recalls

Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS BRAHMS PROCALCITONIN 60T Recalled by Biomerieux Inc Due...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ASTUTE REAGENT ASTUTE ELECTRONIC QUALITY CTRL DEVICE US Recalled by...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30 Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GN73 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 (6X1.8ML) Recalled by Biomerieux Inc...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: API 20 E 25 STRIPS Recalled by Biomerieux Inc Due to As the temperature and...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS PROGESTERONE 60 TESTS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: API STAPH 25 STRIPS+25 MEDIA Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to When selecting...

The Issue: When selecting the site fraction group for treatment, the User may select...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Foundation Medicine, Inc.

Recalled Item: FoundationOne CDx (F1CDx) Recalled by Foundation Medicine, Inc. Due to...

The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Foundation Medicine, Inc.

Recalled Item: FoundationOne Liquid CDx (F1LCDx) Recalled by Foundation Medicine, Inc. Due...

The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· ENDO Pharmaceuticals Solutions, Inc.

Recalled Item: 9 Gauge Disposable Trocars with Blunt Pushers for Use with Recalled by ENDO...

The Issue: No expiration dates printed on the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...

The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Corin Ltd

Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...

The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2022· Companion Medical, Inc.

Recalled Item: InPen Diabetes Management App Recalled by Companion Medical, Inc. Due to...

The Issue: Diabetes management app may crash immediately upon opening, while using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2022· R & D Systems, Inc.

Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...

The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...

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

Class III — Low RiskOngoing
Medical DeviceNovember 7, 2022· Cordis US Corp

Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...

The Issue: There is a potential for separation at the male connector.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2022· Getinge Usa Sales Inc

Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...

The Issue: The power backup battery, under certain conditions, may exhibit reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

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

Class II — Potential Health HazardOngoing