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. 2,439 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,439 in last 12 months

Showing 4708147100 of 52,647 recalls

Medical DeviceSeptember 13, 2013· Mesa Laboratories, Inc.

Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...

The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2013· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....

The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...

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

Class II — Potential Health HazardOngoing
FoodSeptember 12, 2013· Dutch Valley Food Development Inc.

Recalled Item: Roasted Salted Mixed Nuts w/ Peanuts Recalled by Dutch Valley Food...

The Issue: Roasted Salted Mixed Nuts with Peanuts were recalled for undeclared tree...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2013· Dutch Valley Food Development Inc.

Recalled Item: Honey Roasted Peanuts Recalled by Dutch Valley Food Development Inc. Due to...

The Issue: Honey Roasted Peanuts were recalled due to undeclared milk (lactose) and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Convergent Dental

Recalled Item: Solea 1.0 Laser Surgical instrument for use in general and Recalled by...

The Issue: Specific error condition could lead to unintended laser emission during...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Maquet Medical Systems USA

Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...

The Issue: It has come to the attention of MAQUET that in certain rare instances, the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 11, 2013· Physicians Total Care, Inc.

Recalled Item: Loratadine 24 HR-OTC Recalled by Physicians Total Care, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Affected lot numbers may contain...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 11, 2013· Janssen Pharmaceuticals, Inc.

Recalled Item: Risperdal CONSTA (risperiDONE) Recalled by Janssen Pharmaceuticals, Inc. Due...

The Issue: Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...

The Issue: There is a potential issue on running Artis systems running software VC1x...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Leica Microsystems, Inc.

Recalled Item: Leica Ceiling Mount MSF-1 for use with M841 and M501 Recalled by Leica...

The Issue: The ceiling mount supplier encountered an event in which the drive screw in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Leica Microsystems, Inc.

Recalled Item: Leica Ceiling Mount MS-1F & MC-1F for use with the Recalled by Leica...

The Issue: The ceiling mount supplier encountered an event in which the drive screw in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· ArjoHuntleigh Inc.

Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...

The Issue: The lock pin can become stuck in the "in" position during the manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Harvest Technologies Corporation

Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...

The Issue: Potential for leur connector to leak or have cracks.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· SonoSite, Inc.

Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...

The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...

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

Class II — Potential Health HazardOngoing
FoodSeptember 10, 2013· Talenti Gelato

Recalled Item: Talenti German Chocolate Cake Gelato Recalled by Talenti Gelato Due to...

The Issue: Product contains undeclared Allergen; Almonds.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Steris Corporation

Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...

The Issue: STERIS has identified that the population of the G. stearothermophilus...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Aesculap, Inc.

Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...

The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...

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

Class II — Potential Health HazardOngoing