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. 2,769 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,769 in last 12 months

Showing 281300 of 52,647 recalls

Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) TOTE ABRAMS KNEE ARTHROSCOPY Recalled by...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) ARTHROSCOPY CDS Recalled by Medline Industries,...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT UROLOGY SLING Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Surgical Drapes: 1) SHEET Recalled by Medline Industries, LP Due to...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX ST100 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
DrugJanuary 6, 2026· Encon Safety Products Co

Recalled Item: AQ 120 GFEW Recalled by Encon Safety Products Co Due to cGMP deviations.

The Issue: cGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· Straumann USA LLC

Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...

The Issue: The mix up of the impression caps provided in the package. The provided...

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

Class III — Low RiskOngoing
FoodJanuary 6, 2026· Herbs Forever

Recalled Item: HerbsForever- Hingwastika Churna Recalled by Herbs Forever Due to Undeclared...

The Issue: Potential undeclared allergen ingredient (Wheat)

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 6, 2026· Herbs Forever

Recalled Item: HerbsForever- Gastro Care Recalled by Herbs Forever Due to Undeclared Allergen

The Issue: Potential undeclared allergen ingredient (Wheat)

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2026· Medline Industries, LP

Recalled Item: Medline Sterile Saline Wound Wash Recalled by Medline Industries, LP Due to...

The Issue: Medline has identified that the manufacturer of the sterile saline wound...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION Recalled by Medline...

The Issue: Medline has identified that the manufacturer of the sterile saline wound...

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

Class II — Potential Health HazardOngoing