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. 2,563 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,563 in last 12 months

Showing 2450124520 of 53,342 recalls

Medical DeviceDecember 19, 2018· Boston Scientific Corporation

Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...

The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...

The Issue: Evidence supports that when customers performed a fuse replacement as part...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...

The Issue: A software update is being issued to correct multiple issues identified in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· XTANT MEDICAL INC

Recalled Item: Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC Recalled...

The Issue: This recall has been initiated due to a change in packaging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Associates of Cape Cod, Inc.

Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...

The Issue: The kits may contain the incorrect number of components or the kits may be...

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

Class II — Potential Health HazardOngoing
DrugDecember 19, 2018· Teva Pharmaceuticals USA

Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2018· Insulet Corporation

Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...

The Issue: There is a potential for a communication interruption following a bolus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 6cm - Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
FoodDecember 18, 2018· Produce Packaging Inc

Recalled Item: Produce Packaging Recalled by Produce Packaging Inc Due to Potential E. coli...

The Issue: Firm received notification from supplier of potential for contamination with...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2018· Produce Packaging Inc

Recalled Item: Produce Packaging Recalled by Produce Packaging Inc Due to Potential E. coli...

The Issue: Firm received notification from supplier of potential for contamination with...

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

Class I — Serious Health HazardOngoing
Refund