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. 2,639 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,639 in last 12 months

Showing 1750117520 of 52,647 recalls

Medical DeviceJanuary 15, 2021· Biomet, Inc.

Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2021· Bard Peripheral Vascular Inc

Recalled Item: BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm Recalled by Bard...

The Issue: Due to the Penetration Depth Switch used to select the desired penetration...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2021· Physio-Control, Inc.

Recalled Item: PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2...

The Issue: Due to complaints received regarding missing lid magnets which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products VersaTips - Product Usage: used to dispense...

The Issue: A deformity affecting a specific lot of VITROS¿ Chemistry Products...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2021· Medical Components, Inc dba MedComp

Recalled Item: Power Injectable CT Port insertion kits - Product Usage: is Recalled by...

The Issue: The 5F Dignity CT Port kits were packaged with the incorrect size port. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2021· Covidien Llc

Recalled Item: Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm Recalled by...

The Issue: incorrect device is contained in the package. The packaging label indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2021· Silk Road Medical Inc

Recalled Item: ENROUTE Transcarotid Stent System Recalled by Silk Road Medical Inc Due to...

The Issue: Due to complaints received that the tip/nose cone may detach from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2021· Shent USA, Inc.

Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling

The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2021· Shent USA, Inc.

Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling

The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2021· Natus Manufacturing Limited

Recalled Item: Recalled by Natus Manufacturing Limited Due to The external drainage system...

The Issue: The external drainage system failed to meet Pyrogen test requirements for...

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

Class II — Potential Health HazardOngoing
DrugJanuary 11, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: Incorrect Labeling: Incorrect lot number on secondary packaging

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 11, 2021· C.R. Bard, Inc.

Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...

The Issue: The device catheter tip was cut off (no tip) and the product packaging was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Ecolab Inc

Recalled Item: Slush + Warmer Disc Drape Recalled by Ecolab Inc Due to Slits were...

The Issue: Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for Recalled...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
FoodJanuary 10, 2021· Lancaster Foods LLC

Recalled Item: Lancaster Squash Planks Recalled by Lancaster Foods LLC Due to Potential...

The Issue: Product is potentially contaminated with Listeria Monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2021· Lancaster Foods LLC

Recalled Item: Lancaster Butternut Squash Noodles 12 oz.(340g) Recalled by Lancaster Foods...

The Issue: Product is potentially contaminated with Listeria Monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2021· Lancaster Foods LLC

Recalled Item: Own Brands Recalled by Lancaster Foods LLC Due to Potential Listeria...

The Issue: Product is potentially contaminated with Listeria Monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2021· Lancaster Foods LLC

Recalled Item: Own Brands Recalled by Lancaster Foods LLC Due to Potential Listeria...

The Issue: Product is potentially contaminated with Listeria Monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund