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. 2,622 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,622 in last 12 months

Showing 2044120460 of 53,342 recalls

DrugDecember 20, 2019· Assurance Infusion

Recalled Item: TRIMIX FORTE PLUS 30MG/4MG/40MCG/ML INJ in 1 mL vial Assurance Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: SUFENTANIL 300MCG/ML INJ in 20 mL syringe Assurance Infusion (713)-533-8800...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BUP 2.5MG/FENT 25MCG/HYDRO 2MG/MORP 40MG/ML in 20 mL syringe Assurance...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BUP 35MG/FENT 1.5MG/ML in 20 mL syringe Assurance Infusion (713) 533-8800...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: TRIMIX (UA) 30MG/1MG/20MCG/ML INJ in 1 mL vial Assurance Infusion Recalled...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: TESTOSTERONE CYP 200MG/ML OIL (SESAME) INJ in 10 mL vial Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BUP 15MG/CLON 300MCG/ FENT 1500MCG/ML(40) INJ in 20 mL syringe Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: HYDROMORPHONE 3MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: TESTOSTERONE CYP 200MG/ML OIL INJ in 10 mL vial Assurance Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: HYDROMORPHONE 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: CLON 750MCG/MORP 30MG/SUF 37.5MCG/ML in 20 mL syringe Assurance Infusion...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BAC 225MCG/ BUP 4.5MG/ CLON 9MCG/ MORP 3MG/ML ML INJ Recalled by Assurance...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2019· EMESA FOODS CO

Recalled Item: Emesa Foods Premium Sesame Tahini Recalled by EMESA FOODS CO Due to...

The Issue: product tested positive for salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 20, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Lipase Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Firm has received customer complaints regarding failed calibrations and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1 Recalled by...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: PICC Set- PR-35052-HPHNM Recalled by Arrow International Inc Due to Product...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1 Recalled by...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow Central Venous Catheterization Kit ASK-04200-UPM Recalled by Arrow...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT JH-05500 Recalled by Arrow International...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing