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. 2,445 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,445 in last 12 months

Showing 4490144920 of 52,647 recalls

DrugApril 1, 2014· Hi-Tech Pharmacal Co., Inc.

Recalled Item: HydrOXYzine Hydrochloride Oral Solution Recalled by Hi-Tech Pharmacal Co.,...

The Issue: Failed Impurity/Degradation Specification; out-of-specification result for...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2014· Wockhardt Usa Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Wockhardt Usa Inc....

The Issue: Failed Dissolution Specifications: failure of dissolution test observed at...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2014· Zimmer, Inc.

Recalled Item: TRABECULAR METAL MODULAR ACETABULAR SYSTEM Recalled by Zimmer, Inc. Due to...

The Issue: The shell was missing the locking ring.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray...

The Issue: Siemens Radiation Oncology became aware that customers may be using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: Pipeline Embolization Device (PED). Used endovascular treatment of adults...

The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips Medical Systems Computed Tomography X-ray systems (Brilliance CT...

The Issue: A customer reported that the table top had become free floating. A Field...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Ortho Development Corporation

Recalled Item: PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due...

The Issue: A femoral component containing pegs was found in a box for the pegless version.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: 550 TxT Treatment Table of the Digital Linear Accelerator (LINAC) Recalled...

The Issue: Table may lose calibration during patient treatment, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: Alligator Retrieval Device (ARD). Used in the peripheral and...

The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 31, 2014· Vidacare Corporation

Recalled Item: EZ-IO 45mm (40kg & up) Needle Set Recalled by Vidacare Corporation Due to...

The Issue: The voluntary recall is due to the needle set not meeting its specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2014· RGI Medical Manufacturing, Inc.

Recalled Item: Henora 300psi I.V. Catheter Extension Set Product Usage: Recalled by RGI...

The Issue: Problem with low adhesion of the tubing to luer connection which may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2014· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Recalled by...

The Issue: Urgent Device Correction notifications are being sent to USA distributors...

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

Class II — Potential Health HazardOngoing
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: MOJO RISEN Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA; Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: Black Ant Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: AFRICAN BLACK ANT Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: XZEN PLATINUM Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: Xzen 1200 Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: XZEN GOLD Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: XZONE GOLD Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: Xzone 1200 Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund