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. 1,019 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,019 in last 12 months

Showing 32101–32120 of 52,647 recalls

FoodMarch 27, 2017· Whole Food Market

Recalled Item: Whole Foods Market Made Right Here 6pk Banana Choc Chip Muffins Recalled by...

The Issue: Product contains undeclared walnuts

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 27, 2017· Alcon Research, Ltd.

Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...

The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Remel Inc

Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...

The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Teleflex Medical

Recalled Item: WECK Visistat 35R Disposable Skin Stapler Recalled by Teleflex Medical Due...

The Issue: Some boxes are labeled as containing Visistat Wide devices, when they in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Merit Medical Systems, Inc.

Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...

The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Sysmex America Inc

Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...

The Issue: Reported customer complaints of automated hematology analyzers catching fire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Toshiba American Medical Systems

Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...

The Issue: It was discovered during a procedure that when the operator made an exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Tosoh Bioscience Inc

Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...

The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...

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

Class II — Potential Health HazardOngoing
FoodMarch 22, 2017· Whiskey Hill Smokehouse

Recalled Item: Elk Jerky Recalled by Whiskey Hill Smokehouse Due to Undeclared Soy

The Issue: Elk jerky is recalled due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 22, 2017· Whiskey Hill Smokehouse

Recalled Item: Kangaroo jerky Recalled by Whiskey Hill Smokehouse Due to Undeclared Soy

The Issue: kangaroo jerky is recalled due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund