New Mexico recalls
3855 federal recalls on file affecting New Mexico - 230 New Mexico-specific plus 3625 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo surgical burr recalled for breakage risk
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceSurgify MedicalClass IINationwideSurgify Halo burr recalled for breakage risk in spinal surgery
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- 2026-07-01FDA-DeviceIPG MedicalClass IINationwideIPG Medical Thuvera Laser Console recalled for false error display
Software anomaly that causes a false display of error code 5018.
- 2026-07-01FDA-DeviceStrykerClass IINationwideStryker INZONE coil detachment device recalled for battery failure
Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be unable to detach a coil as intended, which may necessitate medical intervention if the procedure must be completed with an alternative technique.
- 2026-07-01FDA-DeviceZimmer BiometClass IINationwideZimmer reamer guide recalled for breakage during use
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
- 2026-07-01FDA-DeviceZimmer BiometClass IINationwideZimmer shoulder reamer guide recalled for breakage risk
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
- 2026-07-01FDA-DeviceVentec Life SystemsClass IINationwideVentec VOCSN+Pro ventilator recalled for backup alarm failure
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.
- 2026-07-01FDA-DevicePhilipsClass IINationwidePhilips Avalon FM20 Fetal Monitor recalled for speaker connector defect
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
- 2026-07-01FDA-DeviceIntuitive SurgicalClass IINationwideIntuitive Surgical Da Vinci recalled for E-brake failure risk
Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs out it may cause restricted column range of motion and/or uncontrolled motion, which may cause patient tissue injury/crushing injury/bleeding.
- 2026-07-01FDA-FoodCerelesClass INationwidePearl Milling Company Original Pancake & Waffle Mix Complete (Mezcla Para Panqueques y Waffles) Net Wt 5.99 oz (170 g). Packed in 50 - 5.99 oz BOPP Pouch units per master case. Keep in a cool, dry place.
Undeclared allergens: Milk and Soy
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).
Potential Salmonella contamination
- 2026-07-01FDA-FoodChampion FoodsClass IINationwideMotor City Pizza Co. 5 Cheese Bread recalled for Salmonella risk
potential salmonella contamination
- 2026-07-01FDA-DrugSun PharmaceuticalClass IINationwideSun Pharmaceutical Perampanel recalled for tablet strength mix-up
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.
- 2026-07-01FDA-DrugElevate Oral CareClass IINationwideElevate Oral Care Povi-One recalled for sub-potency
sub potency
- 2026-07-01FDA-DrugAnnora PharmaClass IINationwideCamber Lacosamide tablets recalled for Selexipag mix-up
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep FREPP Clear recalled for sterility concerns
Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep Clear recalled for fungal contamination risk
Non-Sterility: Due to presence of Aspergillus penicillioides.
- 2026-07-01FDA-DrugCareFusionClass IINationwideBD ChloraPrep FREPP Clear recalled for sterility risk
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
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