New Mexico recalls
3601 federal recalls on file affecting New Mexico - 226 New Mexico-specific plus 3375 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-05-21CPSCHomeProGymNationwideHomeProGym resistance bands recalled for separation hazard
The recalled resistance bands can forcefully separate from the handle during use, posing a risk of serious injury from impact hazard.
- 2026-05-21CPSCABC TradingNationwideABC Trading toys recalled for button battery ingestion risk
The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 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
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