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 2944129460 of 52,647 recalls

Medical DeviceSeptember 13, 2017· Medtronic Vascular, Inc.

Recalled Item: Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm...

The Issue: It was determined that the deflection length indicated on the Guide catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· Abbott Point Of Care Inc.

Recalled Item: i-STAT DE handheld data processing module for clinical use Recalled by...

The Issue: Issues resulting from upgrade to software version 2.8: (1) Location,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· Zoll Manufacturing Corp.

Recalled Item: LifeVest Wearable Defibrillator Model 4000 Recalled by Zoll Manufacturing...

The Issue: Incorrect service code for properly catching critical defects during...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse...

The Issue: Analysis of the difference between the actual device longevity and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim DRG Implantable Pulse Generator Model 3664 Recalled by St. Jude...

The Issue: Analysis of the difference between the actual device longevity and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is...

The Issue: During an examination images were displayed on the live monitor,but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Recalled...

The Issue: Analysis of the difference between the actual device longevity and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2017· Zimmer Biomet, Inc.

Recalled Item: BlockAid Cut Resistant Surgical Glove Liners Recalled by Zimmer Biomet, Inc....

The Issue: Cut resistant surgical glove liners lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2017· Sysmex America, Inc.

Recalled Item: Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets Recalled...

The Issue: There is potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
FoodSeptember 7, 2017· Garden Of Life, LLC

Recalled Item: Garden of Life Recalled by Garden Of Life, LLC Due to The product may pose a...

The Issue: The product may pose a choking hazard to newborns due to the thickness of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 7, 2017· Radiometer America Inc

Recalled Item: AutoCheck5+ Recalled by Radiometer America Inc Due to Radiometer has...

The Issue: Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2...

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

Class II — Potential Health HazardOngoing
DrugSeptember 5, 2017· Teva Pharmaceuticals USA

Recalled Item: Acarbose Tablets Recalled by Teva Pharmaceuticals USA Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 5, 2017· Genentech, Inc.

Recalled Item: Activase (alteplase) Recalled by Genentech, Inc. Due to...

The Issue: Non-Sterility:presence of cracked or chipped glass at the neck of Sterile...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 5, 2017· NOW Foods

Recalled Item: Organic Coconut Sugar Recalled by NOW Foods Due to Undeclared Gluten

The Issue: Undeclared gluten found in the product and the product is labeled "Gluten Free".

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 5, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Assorted Muffins 4-Pack-18 oz. (1 lb. 2 oz.) 510g Recalled by...

The Issue: 4-pack may contain banana nut muffin containing walnuts, allergen-walnuts...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿¿ ¿¿¿ ¿¿¿...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Portex Unit Dose 5 ml Normal Saline (0.9%)¿¿¿¿ ¿ Recalled by Medex...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 5, 2017· Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

Recalled Item: Intermed 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ ¿¿¿ Recalled...

The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...

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

Class I — Serious Health HazardOngoing