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. 2,493 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,493 in last 12 months

Showing 3916139180 of 52,647 recalls

Medical DeviceAugust 4, 2015· MicroPort Orthopedics, Inc.

Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...

The Issue: Unexpected rate of postoperative fractures resulting in the need for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2015· Salter Labs

Recalled Item: NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap...

The Issue: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and...

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

Class II — Potential Health HazardOngoing
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula C&F packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2015· HoneyCombs Industries, LLC

Recalled Item: Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...

The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2015· Liquid Coffee Inc

Recalled Item: Concentrated coffee packed in 1/2 gallon or 1 gallon hermetically Recalled...

The Issue: The pH level in coffee product was elevated above 4.6.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Rivastigmine Tartrate Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 3, 2015· Ferno-Washington Inc

Recalled Item: Ferno iNX Wheeled Stretcher Recalled by Ferno-Washington Inc Due to Hole...

The Issue: Hole elongation in the telescoping load frame channel. A hole elongation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Applied Medical Resources Corp

Recalled Item: Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: Recalled...

The Issue: Potential to improperly characterize tissue within the jaws, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Edward Lifesciences, Llc

Recalled Item: Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer....

The Issue: Flow restriction issues in a trifurcated IV set included in the pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Covidien LLC

Recalled Item: Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Recalled...

The Issue: Infant Heel warmers may break during activation resulting in spillage of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Covidien LLC

Recalled Item: Covidien Argyle Infant Heel Warmers (no tab) Item Code: MH00002N Recalled by...

The Issue: Infant Heel warmers may break during activation resulting in spillage of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: Siemens Intevo Series system Recalled by Siemens Medical Solutions USA, Inc....

The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: Siemens Symbia S Series system Recalled by Siemens Medical Solutions USA,...

The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: Siemens Symbia T Series Recalled by Siemens Medical Solutions USA, Inc. Due...

The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2015· Arrow International Inc

Recalled Item: Arrow International Recalled by Arrow International Inc Due to saline...

The Issue: saline leakage from unsecured connections between the Touhy Borst adaptor...

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

Class II — Potential Health HazardOngoing