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. 2,716 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,716 in last 12 months

Showing 61416160 of 53,342 recalls

Medical DeviceApril 18, 2024· BD SWITZERLAND SARL

Recalled Item: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Recalled by BD...

The Issue: Due to infusion set tubing drip chamber becoming detached from the tubing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Stryker Neurovascular

Recalled Item: The Synchro SELECT Guidewires are a steerable guidewire family with Recalled...

The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Stryker Neurovascular

Recalled Item: The Synchro Neuro Guidewires are a steerable guidewire family with Recalled...

The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Olympus Corporation of the Americas

Recalled Item: OES 4000 Hysteroscope Recalled by Olympus Corporation of the Americas Due to...

The Issue: The required leakage test was not performed following of a re-work for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· Boston Scientific Neuromodulation Corporation

Recalled Item: Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG:...

The Issue: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2024· OptumHealth Care Solutions LLC

Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...

The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...

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

Class I — Serious Health HazardOngoing
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion Recalled by ARG...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 17, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Syringes labeled as: a) SYR 10ML L/L CONTROL Recalled by MEDLINE INDUSTRIES,...

The Issue: These syringes were identified to be affected by the FDA Safety Alert issued...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Blood Pump Rotor Recalled by Fresenius Medical Care Holdings, Inc. Due to An...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing