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 1878118800 of 53,342 recalls

DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Progesterone 300 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Yohimbine HCL 5.4mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Calcium citrate tetrahydrate USP powder Recalled by MasterPharm LLC Due to...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: D-Biotin 300 mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Tadalafil 12 mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Tadalafil 18 mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Tadalafil 3 mg Capsule Recalled by MasterPharm LLC Due to Lack of Processing...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Minoxidil/Biotin/Spironolactone 1.25/5/25mg capsules Recalled by MasterPharm...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Tadalafil 26 mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Vardenafil 20 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Estriol 8 mg Capsule Recalled by MasterPharm LLC Due to Lack of Processing...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Superpotent Drug: Out-of-specification (OOS) result observed in an assay...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2020· Hostess Brands, LLC

Recalled Item: Hostess Raspberry Zingers Recalled by Hostess Brands, LLC Due to Product...

The Issue: Product potentially has mold prior to best by date.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 2, 2020· Whirlpool Corporation

Recalled Item: PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1 Recalled by...

The Issue: The rivets that secure the elastic headband to the face shield have the...

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

Class II — Potential Health HazardOngoing
DrugJuly 1, 2020· Spartan Chemical Co Inc

Recalled Item: Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial)...

The Issue: Microbial contamination of non-sterile products: positive microbial...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 1, 2020· Preferred Pharmaceuticals, Inc.

Recalled Item: Lidothol Patch Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP Deviations: Contract Manufacturing Organization (CMO) misplaced/lost...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2020· ICU Medical, Inc.

Recalled Item: 6' (15 cm) Appx 0.09 ml Recalled by ICU Medical, Inc. Due to Incorrect...

The Issue: Incorrect filter assemblies in IV administration set.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 - Product Usage: is intended Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 - Product Usage: is intended Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris SpO2 Module Model 8210 and Model 8220 - Product Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing