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. 2,348 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,348 in last 12 months

Showing 2166121680 of 47,027 recalls

Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
FoodApril 11, 2019· Patagonia Provisions Inc

Recalled Item: Patagonia Provisions Classic Barbecue Savory Seeds Recalled by Patagonia...

The Issue: Products are labeled gluten free but have been found to contain gluten in...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 11, 2019· Patagonia Provisions Inc

Recalled Item: Patagonia Provisions Savory Seeds Variety Pack Recalled by Patagonia...

The Issue: Products are labeled gluten free but have been found to contain gluten in...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 11, 2019· Patagonia Provisions Inc

Recalled Item: Patagonia Provisions Mellow Curry Savory Seeds Recalled by Patagonia...

The Issue: Products are labeled gluten free but have been found to contain gluten in...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 11, 2019· Patagonia Provisions Inc

Recalled Item: Patagonia Provisions Chipotle Lime Savory Seeds Recalled by Patagonia...

The Issue: Products are labeled gluten free but have been found to contain gluten in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 10, 2019· Becton Dickinson & Company

Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...

The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...

The Issue: The firm has become aware of a potential problem that their Catheters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...

The Issue: The firm has become aware of a potential problem that their Catheters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Uromedica Inc.

Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...

The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing