Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1828118300 of 53,342 recalls

DrugAugust 24, 2020· Strides Inc.

Recalled Item: Strides Pharma Inc.Potassium Chloride Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2020· Teva Pharmaceuticals USA

Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Sub-Potent Drug: Out of specification test results for potency (below...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2020· Boston Scientific Corporation

Recalled Item: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) Recalled by...

The Issue: Opticross 35 Peripheral Imaging Catheter is being recalled because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Alcon Research, LLC

Recalled Item: Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health"...

The Issue: The third-party brand latex micro surgical gloves packaged within specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Irvine Biomedical Inc, a St. Jude Medical Co.

Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...

The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Irvine Biomedical Inc, a St. Jude Medical Co.

Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...

The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Imactis

Recalled Item: Imactis Patient Fiducial (Patient ) Recalled by Imactis Due to The firm has...

The Issue: The firm has received reports concerning the patient fiducial disk...

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

Class II — Potential Health HazardOngoing
FoodAugust 22, 2020· Russ Davis Wholesale, LLC

Recalled Item: Peach Salsa Recalled by Russ Davis Wholesale, LLC Due to Potential...

The Issue: Peach Salsa was made with peaches may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 21, 2020· Handicare AB

Recalled Item: SwiftHook sold as the following: a. Individually as SwiftHook b. Recalled by...

The Issue: Carry bar may detach during use of mobile lifts and ceiling lifts equipped...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2020· North American Rescue LLC.

Recalled Item: 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171 Recalled...

The Issue: Lack of sterility assurance of the 30-0171

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Anti-TPO Assay on cobas e analyzers 411 Recalled by Roche...

The Issue: Recent internal verification studies found the current RF interference claim...

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

Class II — Potential Health HazardOngoing
DrugAugust 19, 2020· BAYSHORE PHARMACEUTICALS

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2020· BAYSHORE PHARMACEUTICALS

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 19, 2020· Wawona Packing Co LLC dba Prima Wawona

Recalled Item: Fresh peaches - sold loose/bulk and Bagged fresh peaches Recalled by Wawona...

The Issue: Trace back information in an outbreak of Salmonella Enteritidis shows...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 19, 2020· Ansell Healthcare Products LLC

Recalled Item: MICROFLEX Diamond Grip Examination Gloves Recalled by Ansell Healthcare...

The Issue: Examination gloves were shipped inadvertently, without to verify barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension LOCI High Sensitivity Troponin I (TNIH) Flex reagent...

The Issue: Positive bias across the Analytical Measurement Range of the TNIH assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Software: Syngo.via RT Image Suite software version VA30_SP02 with license...

The Issue: Calibration offset between the central CT image plane and the external RT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing