Vermont recalls
3490 federal recalls on file affecting Vermont - 115 Vermont-specific plus 3375 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-05-20FDA-PRHometown FoodNationwideBirch Benders pancake mix recalled for undeclared egg
Chicago (May 20, 2026) – Hometown Food Company, in cooperation with Element Food Solutions, today initiated a limited, voluntary recall of a single lot code of its Birch Benders 12oz Sweet Potato Pancake Mix because it may contain undeclared egg. People who have an allergy or severe sensitivity to e
- 2026-05-20FDA-DeviceMedtronicClass IINationwideMedtronic SynchroMed programmer software recalled for scheduling error
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.
- 2026-05-20FDA-DeviceMicroventionClass IINationwideMicroVention LVIS stent recalled for sizing defect risk
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to increased vessel wall stress, neointimal hyperplasia, vessel injury/rupture; if undersized may lead to incomplete expansion/malposition, acute stent thrombosis, distal embolization, ischemic neurological events
- 2026-05-20FDA-DeviceStrykerClass IINationwideMedtronic Marinr catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideDaig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker electrophysiology catheter recalled for seal defect
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker electrophysiology catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker electrophysiology catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD EP XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD EP XT catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic XT catheters recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic Tip Steerable recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceIntegra LifeSciencesClass IINationwideCodman CerebroFlo EVD Catheter recalled for endotoxin contamination
Out-of-specification endotoxin result that did not meet the acceptance criteria.
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