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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 2708127100 of 29,284 recalls

Medical DeviceMay 1, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...

The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...

The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· CooperSurgical, Inc.

Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...

The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Elekta, Inc.

Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...

The Issue: It is possible for an intermittent error to occur in the gantry sensor of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Elekta, Inc.

Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...

The Issue: Unexpected movement during beam delivery may not be detected if there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· American Optisurgical Inc

Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....

The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Medication Cup. For the delivery of liquid medications Recalled...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 350. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· American Optisurgical Inc

Recalled Item: TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1...

The Issue: American Optisurgical, Inc. is recalling certain lots of TX1 Tissue Removal...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· TZ Medical Inc.

Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...

The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2013· Biomet, Inc.

Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...

The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Beckman Coulter Inc.

Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...

The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Heart Sync, Inc

Recalled Item: Heart Sync C100-Physio Radiotransparent Defibrillation Electrodes Monophasic...

The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...

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

Class II — Potential Health HazardOngoing