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. 2,520 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,520 in last 12 months

Showing 3506135080 of 52,647 recalls

Medical DeviceJune 29, 2016· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: ArjoHuntleigh Sara Combilizer Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....

The Issue: ArjoHuntleigh has concluded that a device tipping hazard may occur on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· C.R. Bard, Inc.

Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem

The Issue: Labeling problem

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

Class III — Low RiskOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· CHG Hospital Beds Inc

Recalled Item: Spirit Select Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical...

The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Medtronic Xomed, Inc.

Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to Wire in...

The Issue: Wire in tubing can become exposed, posing potential harm to the intubated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· B-K Medical A/S

Recalled Item: BK Medical ApS Ultrasound System Scanner bk2300 - Model #: Recalled by B-K...

The Issue: In the system (bk3500) software generic volume measurement (HxWxLxl)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· CHG Hospital Beds Inc

Recalled Item: Spirit Plus Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical is...

The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2016· Golden State Medical Supply Inc.

Recalled Item: DULOXETINE Delayed-Release Capsules Recalled by Golden State Medical Supply...

The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Recalled...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set Recalled by ConMed...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Trumpet Handpiece only Recalled by ConMed Corporation Due to The...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2016· ConMed Corporation

Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or...

The Issue: The packaging seal may contain a crease. The crease may result in an open...

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

Class II — Potential Health HazardOngoing