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. 2,631 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,631 in last 12 months

Showing 1644116460 of 29,284 recalls

Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KIT00713 KIT BY PASS Product Usage: The Endo GIA Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX KITDE0183 APPENDIX LIPPE DETMOLD (KITDE0183) (2) KIT-DE-0083...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm - Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX HEMIGX1 ZESTAW DO HEMICOLECTOMII (Item Number HEMIGX1 ZESTAW DO...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX PST01199 BARIATRIC TRISTAPLE (Item Number: PST01199) (2) BOX PST03403...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1) BOX 01KBAR006116V PROC BYPASS 01KBAR0061(Item Code 01KBAR006116V PROC...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX TGGLOGOWX1 DO TOTAL GASTRECTOMIII Product Usage: The Endo GIA Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX LAPIMBGP1 ZESTAW DO MGBP (LAPIMBGP1) Product Usage: The Endo Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KIT00714 KIT SLEEVE Product Usage: The Endo GIA universal Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)LAPBARLECZNA ZESTAW BARIATRYCZNY LECZNA (2) KITBAR021- BARIATRIC KIT X1...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX1073076GASB1 BBR GASTRIC BYPASS S(Item Code BOX1073076GASB1 BBR GASTRIC...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX Pentra Micro ALBUMIN 2 CP Recalled by Horiba Instruments, Inc dba Horiba...

The Issue: When the ABX Pentra Micro ALBUMIN 2 CP (ALBT2) Reagent 2 is sampled and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VMIN ZESTAW DO VATS PODSTAWOWY Product Usage: The Endo Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm- 3.5mm(...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VATS1SCDX DO ZABIEGOW VATS Product Usage: The Endo GIA Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX PST04089 SLEEVE AIWA CLINIC Item Number:PST04089 SLEEVE AIWA CLINIC...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing