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. 2,609 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,609 in last 12 months

Showing 2180121820 of 53,342 recalls

Medical DeviceAugust 19, 2019· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing...

The Issue: Interference can occur between the adolescent attachment bolt and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...

The Issue: Flow cytometers, when used with specific tubes may experience excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...

The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...

The Issue: Discrepancy between the correct expiration dates on the individual pouches...

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

Class III — Low RiskOngoing
DrugAugust 16, 2019· SCA Pharmaceuticals, LLC

Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for Recalled by SCA...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 16, 2019· Kashat Wholesale, Inc.

Recalled Item: Ground Cinnamon 4oz plastic container 24 containers per wholesale case...

The Issue: positive samples for lead in bulk cinnamon

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 16, 2019· Pepsico Inc

Recalled Item: Diet Mountain Dew (Dewnited Michigan) 20 oz. plastic bottle Promotional...

The Issue: Front label states diet Mountain Dew, but the product is actually full...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 16, 2019· IrriMAX Corporation

Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...

The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Bioseal Corporation

Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...

The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...

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

Class II — Potential Health HazardOngoing