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 3016130180 of 52,647 recalls

Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· Xintec Corp

Recalled Item: OptiLITE(TM) Products for Laser Surgery Recalled by Xintec Corp Due to It...

The Issue: It has been determined that the reprocessing instructions may not provide...

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2017· Vitility

Recalled Item: MAN OF STEEL capsules Recalled by Vitility Due to Undeclared Sildenafil

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: QUELICIN (Succinylcholine Chloride) Injection Recalled by Advanced Pharma...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Paroxetine Extended-Release Tablets USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Dissolution Specifications: out of specification observed in...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom HEART CATH TRAY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom SPINE convenience kits Recalled by Avid Medical, Inc. Due to...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· NeuroLogica Corporation

Recalled Item: The GC80 Digital X-ray Imaging System Recalled by NeuroLogica Corporation...

The Issue: An image was obtained with over exposure during a Thorax examination using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom GENERAL PACK convenience kits Recalled by Avid Medical, Inc....

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom SHOULDER ARTHROSCOPY convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom DAVINCI PACK convenience kits Recalled by Avid Medical, Inc....

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom MINOR PROCEDURE 6A convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing