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. 2,609 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,609 in last 12 months

Showing 2146121480 of 53,342 recalls

DrugSeptember 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 300mg 30 Capsules Rx Only...

The Issue: CGMP Deviations: Detection of a trace amount of an unexpected impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Unipharma, Llc.

Recalled Item: DrKids Children's Natural Cough Syrup English Ivy Leaf Recalled by...

The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2019· Tomtec Imaging Systems Gmbh

Recalled Item: TOMTEC-ARENA TTA2 Recalled by Tomtec Imaging Systems Gmbh Due to The firm...

The Issue: The firm discovered a software issue associated with the Image-Com...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Potential for calibration error resulting in QC failures after the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 20, 2019· Akorn, Inc.

Recalled Item: Phenylephrine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...

The Issue: Lack of Assurance of Sterility: Out of specification results for container...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 20, 2019· Roland Foods, LLC

Recalled Item: Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) Recalled by...

The Issue: Potential to be contaminated with Clostridium botulinum.

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 20, 2019· Roland Foods, LLC

Recalled Item: Roland Brand Red Caviar - Whole Grain Lumpfish (Lumpfish Roe) Recalled by...

The Issue: Potential to be contaminated with Clostridium botulinum.

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 19, 2019· Aurobindo Pharma USA Inc.

Recalled Item: Dextroamphetamine Sacharate Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Superpotent Drug: Amphetamine Mixed Salts 20mg have been found to be out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium/ Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium /Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2019· Ra Medical Systems, Inc.

Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...

The Issue: The firm has become aware there is a potential problem with its DABRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/wing 5700LAX...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing