Minnesota recalls
2453 federal recalls on file affecting Minnesota - 142 Minnesota-specific plus 2311 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideCheck your Endo-Model Replacement Plateau implant
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideStop using Waldemar Link Endo-Model Plateau screw
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideStop using affected Waldemar Link plateau screws
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideCheck your Endo-Model Replacement Plateau implant
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideStop using affected Waldemar Link plateau screws
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideContact your surgeon about Waldemar Link plateau screw
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideCheck Waldemar Link knee implant screw
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideCheck Endo-Model SL implant lot numbers
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideCheck Waldemar Link implant screw lot numbers
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideStop using Waldemar Link Endo-Model Plateau screws
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceWaldemar LinkClass IINationwideStop using affected Waldemar Link implant components
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
- 2026-03-18FDA-DeviceExactechClass IIStop using Exactech Equinoxe instrument kits
Impactor handle may be missing cross-pin
- 2026-03-18FDA-DeviceExactechClass IIStop using Exactech Equinoxe Ergo impactor handles
Impactor handle may be missing cross-pin
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa model
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa model number
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa serial number
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa serial number
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa serial number
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa serial number
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa serial number
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwidePenner Pacific Bathing Spa, Model Numbers 360020-1EP
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa serial number
The device does not bear a unique device identifier.
- 2026-03-18FDA-DevicePenner Patient CareClass IIINationwideCheck your Penner Pacific Bathing Spa model
The device does not bear a unique device identifier.
- 2026-03-18FDA-DeviceRaz DesignClass IINationwideStop using affected Raz shower commode chairs
Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.
- 2026-03-18FDA-DeviceIon Beam ApplicationsClass IINationwideContact IBA if you operate PROTEUS 235 proton system
It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS does not interrupt the beam delivery if the Healthy Signal from an external gating device is lost. This may lead to a risk of mistreatment when external gating devices are used.
- 2026-03-18FDA-DeviceBecton DickinsonClass IINationwideCheck BD syringes for packaging error
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
- 2026-03-18FDA-FoodAmbrosiaClass INationwideStop using Rosabella moringa capsules
Product may be contaminated with Salmonella
- 2026-03-18FDA-FoodNovamexClass IIICheck C2O Coconut Water 15-pack boxes for label error
The outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar (5g per 17.5oz can), while the primary packaging (the can) has the correct Nutrition Facts Panel and Ingredient List.
- 2026-03-18FDA-DrugZydusClass IINationwideIcosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. NDC: 70710-1592-7
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
- 2026-03-13USDAPublic Health AlertCheck your La Boulangerie pastry boxes
Misbranding
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