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. 2,542 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,542 in last 12 months

Showing 2598126000 of 52,647 recalls

Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-P160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite 23 GA Vit Cutter Recalled by Bausch & Lomb Inc...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite 20 GA Vit Cutter Recalled by Bausch & Lomb Inc...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite 25 GA Vit Cutter Recalled by Bausch & Lomb Inc...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...

The Issue: The back cap separates from the body of the vitrectomy cutter.

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugAugust 7, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Doxycycline Hyclate USP Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications: manufacturer West-Ward Pharm Corp....

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2018· Natures Bounty Inc

Recalled Item: BLUE GREEN ALGAE: Packaged under the following brands: AMERICAN HEALTH...

The Issue: High level of microcystin observed in the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2018· Medtronic Inc.

Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...

The Issue: There is a potential security vulnerability related to the use of the remote...

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

Class I — Serious Health HazardOngoing