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 2924129260 of 52,647 recalls

FoodOctober 13, 2017· Wegmans Food Markets, Inc.

Recalled Item: 038267 - Wegmans Cheese Danish Twist Recalled by Wegmans Food Markets, Inc....

The Issue: Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 13, 2017· Wegmans Food Markets, Inc.

Recalled Item: 085194 - Wegmans Turnovers Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product contains undeclared FD&C Yellow 5 & Yellow 6, Potassium Sorbate, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 13, 2017· ASK Foods Inc

Recalled Item: taste of Inspirations Classic Red Skin Potato Salad Recalled by ASK Foods...

The Issue: A.S.K. Foods, Inc. of Palmyra, Pennsylvania is voluntarily recalling one lot...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 12, 2017· Genzyme Corporation

Recalled Item: Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection Recalled by Genzyme...

The Issue: Labeling: Incorrect or Missing Package Insert.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

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

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

Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· GE Medical Systems China Co., Ltd.

Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...

The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· GE Medical Systems China Co., Ltd.

Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...

The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...

The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...

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

Class I — Serious Health HazardOngoing
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride...

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
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag 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
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Diltiazem HCL 125 mg added to 0.9% Sodium Chloride 100 ml bag 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
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Norepinephrine Bitartrate16 mg added to 0.9% Sodium Chloride 250 mL bag...

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
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: fentaNYL citrate 1000 mcg (10 mcg/mL) 100 mL Cassette in 0.9% Sodium...

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
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: OXYtocin 30 units added to 0.9% Sodium Chloride 500 mL bag 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
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Norepinephrine Bitartrate 8 mg added to 0.9% Sodium Chloride 250 mL in a bag...

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