Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,332 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,332 in last 12 months

Showing 2476124780 of 47,027 recalls

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: KIT-DE-0080 BYPASS KIT LOHNE X1( Item KIT-DE-0080) Product Usage: The...

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 KITDE0143 BYPASS BOX (Item Number: KITDE0143 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: BOX MGBGLOGX1 ZESTAW MINI GASTRIC BYPASS 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: (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: 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)BOX SLEEVEGK3 (2) BOX SLEEVEGK4 SLEEVE GASTRECTOMY (3)BOX SLEEVEJAWI...

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 60mm -2.5mm...

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: 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: 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: (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 25, 2018· ConvaTec, Inc

Recalled Item: Convatec Esteem(TM) Synergy Stomahesive(R) Recalled by ConvaTec, Inc Due to...

The Issue: It was discovered that the stoma hole of one lots of the Esteem synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Biocare Medical, LLC

Recalled Item: Vulcan Fast Red Chromogen Kit 2 Recalled by Biocare Medical, LLC Due to...

The Issue: Chromogen failed to develop due to a stability issue caused by environmental...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
FoodApril 24, 2018· Labrada Nutrition, Inc

Recalled Item: Lean Pro 8 Cookies & Cream 1 Recalled by Labrada Nutrition, Inc Due to...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund