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Recalls distributed in Minnesota

These notices name Minnesota in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

3,899 stored notices name Minnesota, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.

Medical devices

Reported Apr 22, 2026

iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Gentuity HF-OCT Imaging System Model G10-01; Software version 23.2.13;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Gentuity, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp. (NeuroSciences)

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Philips Spectral CT on Rails. Model Number: 728334.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2026

Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Blueroot Health, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2026

B¿R¿A¿H¿M¿S KRYPTOR compact REACT, REF: 89986, used with B¿R¿A¿H¿M¿S PlGF Plus KRYPTOR, REF: 859075N, and run on the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Brahms GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

BD Kiestra" ReadA; Catalog No.: 446948.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bd Kiestra Lab Automation

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2026

" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Jfe Franchising Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes (USA) Products LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2026

Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ajinomoto Foods North America Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2026

MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

I.T.S. GmbH

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Merit Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2026

SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Savannah Bee Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2026

Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Straumann USA LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2026

Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.