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. 1,077 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,077 in last 12 months

Showing 16881–16900 of 52,647 recalls

Medical DeviceApril 1, 2021· Stryker Leibinger GmbH & Co. KG

Recalled Item: DirectInject consists of a sterile dual paste system which is Recalled by...

The Issue: Inability for the user to inject the paste from the syringe into the target...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD Recalled by Smiths Medical ASD Inc....

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: ELI 280 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: HIGH PRESSURE TUBING Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Gang Cath Lab Set Recalled by Smiths Medical ASD Inc. Due to Specific lots...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: Surveyor S12/S19 Bedside Patient Monitor Recalled by Welch Allyn Inc Mortara...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: LogiCal Monitoring Set Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific lots of...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Tubing with male luer lock adapter (Component) a. 76 cm Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Palm Cups - Product Usage: intended to be used to Recalled by Smiths Medical...

The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: ACE MDI Spacer with Small Mask - Product Usage: designed Recalled by Smiths...

The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...

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

Class II — Potential Health HazardOngoing
DrugMarch 31, 2021· QMart

Recalled Item: IMPERIAL GOLD 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund