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. 2,648 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,648 in last 12 months

Showing 1570115720 of 52,647 recalls

Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-3C40 OES Bronchofiberscope Recalled by Olympus Corporation of the...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-XT160 EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of the...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Biodex Medical Systems, Inc.

Recalled Item: AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08...

The Issue: When deleting a previously entered custom isotope, the software deletes the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-1T60 OES Bronchofiberscope Recalled by Olympus Corporation of the...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-N20 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-P60 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-Q180-AC EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-XP160F EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-P180 EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation of...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.CT VA20A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for data loss when using the contouring or patient marking...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite with syngo.via VB30 Recalled by Siemens Medical...

The Issue: Potential for data loss when using the contouring or patient marking...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A Recalled by...

The Issue: Potential for data loss when using the contouring or patient marking...

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

Class II — Potential Health HazardOngoing
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 0.5mg/1mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Akorn, Inc.

Recalled Item: Betamethasone Dipropionate Lotion USP (Augmented) Recalled by Akorn, Inc....

The Issue: Failed impurities/degradation specification: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· SigmaPharm Laboratories LLC

Recalled Item: Sodium Phenylbutyrate POWDER Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Failed Impurities Specifications: Out of Specification impurity results...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 13, 2021· Hostess Brands, LLC

Recalled Item: Hostess Soft White Hot Dog Buns Recalled by Hostess Brands, LLC Due to...

The Issue: The firm's contract manufacturer found positive environmental samples...

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

Class II — Potential Health HazardOngoing
Refund