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 4040140420 of 52,647 recalls

Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
DrugMay 7, 2015· Teva Pharmaceuticals USA

Recalled Item: QVAR (beclomethasone dipropionate HFA 40 mcg) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 6, 2015· Smith & Nephew, Inc.

Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...

The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Smith & Nephew, Inc.

Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...

The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Biocare Medical, LLC

Recalled Item: D2-40 (Lymphatic Marker) Recalled by Biocare Medical, LLC Due to Firm...

The Issue: Firm discovered that incorrect Instructions for Use were shipped with one...

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

Class III — Low RiskOngoing
Medical DeviceMay 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System (enGen System) Recalled by Ortho-Clinical...

The Issue: Recapper Caps may fall off of, or be knocked from sample tubes placed in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Smith & Nephew, Inc.

Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...

The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Smith & Nephew, Inc.

Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...

The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: The Rapidlab 1265 system is a blood gas analyzer used Recalled by Siemens...

The Issue: D50 and D51 diagnostic error codes are not functional.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Workflow SLR Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential exists for order transactions from interfaced HIS (Hospital...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Signal Reagent Recalled by ORTHO-CLINICAL...

The Issue: The Immunodiagnostic Products Signal Reagent, Lot 3082 as the reagent packs...

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

Class III — Low RiskOngoing
Medical DeviceMay 6, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: The Rapidlab 1260 system is a blood gas analyzer used Recalled by Siemens...

The Issue: D50 and D51 Diagnostic error codes are not functional.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Smith & Nephew, Inc.

Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...

The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...

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

Class II — Potential Health HazardOngoing
FoodMay 6, 2015· Golden Krust Caribbean Bakery, Inc.

Recalled Item: Golden Krust SOYA PATTIES Recalled by Golden Krust Caribbean Bakery, Inc....

The Issue: Golden Krust Caribbean Bakery & Grill has recalled their Jamaican Style...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 6, 2015· Golden Krust Caribbean Bakery, Inc.

Recalled Item: Golden Krust Caribbean JAMAICAN STYLE SHRIMP PATTIES Recalled by Golden...

The Issue: Golden Krust Caribbean Bakery & Grill has recalled their Jamaican Style...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 5, 2015· ResMed Ltd.

Recalled Item: Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator....

The Issue: The Astral device allows clinicians to disable all alarms including those...

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

Class II — Potential Health HazardOngoing