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. 2,647 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,647 in last 12 months

Showing 1642116440 of 53,342 recalls

Medical DeviceApril 14, 2021· Radiometer Medical ApS

Recalled Item: Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 Recalled by...

The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2021· Radiometer Medical ApS

Recalled Item: Radiometer ABL90 FLEX PLUS Analyzer with E3800 PC units. The Recalled by...

The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2021· Beckman Coulter Inc.

Recalled Item: Access SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to specimens...

The Issue: specimens collected in transport media may result is false negative results...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2021· Nomax Inc

Recalled Item: Dry Eye Test Recalled by Nomax Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 13, 2021· Philips North America Llc

Recalled Item: BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended...

The Issue: Cooling Unit (CLU) expelled out of a CT gantry of an iCT system may result...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2021· Edge Pharma, LLC

Recalled Item: Betadine (Povidone-Iodine) 5% Recalled by Edge Pharma, LLC Due to Defective...

The Issue: Defective container; syringe content migrating past the seal of the plunger...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 12, 2021· NATURE'S SUNSHINE PRODUCTS

Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...

The Issue: The firm was notified by an ingredient supplier of Medium Chain...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 12, 2021· NATURE'S SUNSHINE PRODUCTS

Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...

The Issue: The firm was notified by its ingredient supplier of Medium Chain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 12, 2021· Boston Scientific Corporation

Recalled Item: VICI VENOUS STENT System Product Usage: is intended for the Recalled by...

The Issue: The firm has received reports of stent migration after implantation

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 12, 2021· Boston Scientific Corporation

Recalled Item: VICI RDS VENOUS STENT System Product Usage: is indicated for Recalled by...

The Issue: The firm has received reports of stent migration after implantation

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 12, 2021· DJ Orthopedics de Mexico S.A. de C.V.

Recalled Item: DONJOY ULTRASLING PRO ER/IR 30 Recalled by DJ Orthopedics de Mexico S.A. de...

The Issue: failed rivet at the chafe tab of arm sling.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2021· DJ Orthopedics de Mexico S.A. de C.V.

Recalled Item: DONJOY ULTRASLING PRO AB Recalled by DJ Orthopedics de Mexico S.A. de C.V....

The Issue: failed rivet at the chafe tab of arm sling.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2021· DJ Orthopedics de Mexico S.A. de C.V.

Recalled Item: DONJOY PRO Recalled by DJ Orthopedics de Mexico S.A. de C.V. Due to failed...

The Issue: failed rivet at the chafe tab of arm sling.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2021· DJ Orthopedics de Mexico S.A. de C.V.

Recalled Item: DONJOY ULTRASLING PRO ER/IR 15 Recalled by DJ Orthopedics de Mexico S.A. de...

The Issue: failed rivet at the chafe tab of arm sling.

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

Class II — Potential Health HazardOngoing
FoodApril 10, 2021· HOSTESS BRANDS LLC

Recalled Item: Hostesss SnoBalls packaged as Hostess Chocolate CupCakes Recalled by HOSTESS...

The Issue: SnoBalls snack cakes were packaged with a label for Chocolate CupCakes...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2021· Teligent Pharma, Inc.

Recalled Item: Flurandrenolide Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 9, 2021· SPINEART SA

Recalled Item: PERLA TL Lateral Connector Open - Product Usage: intended to Recalled by...

The Issue: Due to external labelling error/mix-up. Affected product external labels...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2021· Avid Medical, Inc.

Recalled Item: FISTULA ON-OFF KIT. Medical convenience kit Recalled by Avid Medical, Inc....

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Avid Medical, Inc.

Recalled Item: DIALYSIS ACCESS Medical convenience kit Recalled by Avid Medical, Inc. Due...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· INNOVA MEDICAL GROUP, INC.

Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 3T Recalled by INNOVA MEDICAL GROUP,...

The Issue: Due to distributing test kits to customers who were not part of a clinical...

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

Class I — Serious Health HazardOngoing