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. 2,574 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,574 in last 12 months

Showing 1912119140 of 29,284 recalls

Medical DeviceFebruary 10, 2017· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...

The Issue: A damaged temperature sensor at the endoscope's tip can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Remel Inc

Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...

The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Smiths Medical ASD Inc.

Recalled Item: Bivona¿ TTS (Tight to Shaft) Pediatric Tracheostomy Tube Recalled by Smiths...

The Issue: Smiths Medical became aware that one lot of the Bivona¿ 3.5mm TTS Cuffed...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...

The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to It has been...

The Issue: It has been observed during testing that there could be clinically...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Del Mar Reynolds Medical, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....

The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Tosoh Bioscience, Inc.

Recalled Item: AIA-PACK TgAb CONTROL SET Recalled by Tosoh Bioscience, Inc. Due to The...

The Issue: The label contains two different methodologies. Quality Control values for...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Tosoh Bioscience, Inc.

Recalled Item: AIA-PACK TPOAb CONTROL SET Recalled by Tosoh Bioscience, Inc. Due to The...

The Issue: The label contains two different methodologies. Quality Control values for...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF#...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing