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. 2,576 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,576 in last 12 months

Showing 1622116240 of 29,286 recalls

Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: UNIQ Product Usage: Vascular Recalled by Philips Healthcare Due to The first...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Philips Healthcare

Recalled Item: Allura Xper Product Usage: Vascular Recalled by Philips Healthcare Due to...

The Issue: The first time an operator selects a new procedure type during a single...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to

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

Class II — Potential Health HazardOngoing