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. 2,532 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,532 in last 12 months

Showing 2750127520 of 53,342 recalls

DrugApril 13, 2018· Boiron Inc.

Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...

The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 13, 2018· St Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...

The Issue: Devices inappropriately displayed a low battery indicator determined to be...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2018· AMA Wholesale

Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Recalled by...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROW JACC with Chlorag+ard Technology Recalled by Arrow International Inc...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Spring-Wire Guide Introducer Catheter Assembly Recalled by Arrow...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit Recalled...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Ninepoint Medical Inc.

Recalled Item: NvisionVLE¿ Low-Profile Optical Probe Recalled by Ninepoint Medical Inc. Due...

The Issue: Distal tips of the probes may detach from the probe shaft during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Arterial Line Kit with Sharps Safety Features and Maximal Barrier...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: 10 cc Luer-Slip Loss of Resistance Syringe Recalled by Arrow International...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: SnapLock" Catheter/Syringe Adapter Recalled by Arrow International Inc Due...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing