Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,011 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,011 in last 12 months

Showing 77417760 of 29,284 recalls

Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Wire Guide (The Firm) Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Torq-Flex Wire Guide Australian Modification Recalled by Cook Incorporated...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Cope Mandril Wire Guide (Stainless Steel) Recalled by Cook Incorporated Due...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Double Flexible Tipped Wire Guide Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Fixed Core Wire Guide Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Amplatz extra Stiff Wire Guide Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Rosen Curved Wire Guide Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Wire Guide (The Firm LT) Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Bentson Plus Wire Guide (Extra Body/20cm Distal Flexibility with Softened...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Newton Wire Guide (LT Taper/10cm Distal Flexibility) Recalled by Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Vinyl Connecting Tube Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Fixed Core Wire Guide (Safe-T-J Curved) Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Encore Medical, LP

Recalled Item: EMPOWER 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Hip...

The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Hip liner...

The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear...

The Issue: Procedure packs contained a recalled product.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· CooperSurgical, Inc.

Recalled Item: Humidifier bottle and syringe filter kit (6 count of each) Recalled by...

The Issue: There is a potential breach to the sterile barrier containing the Humidifier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· CooperSurgical, Inc.

Recalled Item: Humidifier bottle and syringe filter kit (6 count of each) Recalled by...

The Issue: There is a potential breach to the sterile barrier containing the Humidifier...

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

Class II — Potential Health HazardOngoing