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. 968 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
968 in last 12 months

Showing 39081–39100 of 53,342 recalls

FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Onion salt Recalled by PIAZZA PRODUCE, INC. Due to Product labeling does not...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: BBQ Spice Recalled by PIAZZA PRODUCE, INC. Due to Product labeling does not...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Quebec Steak seasoning Recalled by PIAZZA PRODUCE, INC. Due to Undeclared...

The Issue: Product labeling does not contain a listing of ingredients. Undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Quebec Chicken seasoning Recalled by PIAZZA PRODUCE, INC. Due to Undeclared...

The Issue: Product labeling does not contain a listing of ingredients. Undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Bayside Seasoning Recalled by PIAZZA PRODUCE, INC. Due to Product labeling...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Seafood seasoning Recalled by PIAZZA PRODUCE, INC. Due to Product labeling...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Fajita seasoning Recalled by PIAZZA PRODUCE, INC. Due to Undeclared Soybean

The Issue: Product labeling does not contain a listing of ingredients. Undeclared...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Chili Powder Recalled by PIAZZA PRODUCE, INC. Due to Product labeling does...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Cajun seasoning Recalled by PIAZZA PRODUCE, INC. Due to Product labeling...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2015· PIAZZA PRODUCE, INC.

Recalled Item: Hickory Smoke salt Recalled by PIAZZA PRODUCE, INC. Due to Product labeling...

The Issue: Product labeling does not contain a listing of ingredients.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Aortic Punch Catalog Numbers APM40 Recalled by International Biophysics...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Recalled by...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Vascular Loop Catalog Number CH111 Recalled by International Biophysics...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· Carestream Health Inc

Recalled Item: CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a...

The Issue: Software defect that impacts image alignment when using the automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing