State

Minnesota product recalls

73,833 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,851
Critical: 1,137
Severe: 2,246
Most recent: 2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57451–57475 of 81684

HighFDA (Devices)·Z-0133-2016·2015-10-28
Cardinal Health Recalls Ambitex NMD400 Nitrile Exam Gloves Due to Leak Test Failure
Cardinal Health is recalling Ambitex NMD400 Nitrile Exam Gloves (size medium) because samples failed FDA water leak tests, compromising their barrier function.
Product
Ambitex NMD400 Nitrile Exam Gloves size medium. General Hospital and Personal use. Intended to be worn on the hand for medical purposes to provide a barrier against potentially infectious materials and other contaminants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0037-2016·2015-10-28
JBN Growtein Protein Powder Recalled for Unlabeled Milk Allergen
Nutrition Resource Services is recalling JBN Growtein protein powder because whey-based products are not labeled as containing milk.
Product
JBN (Just Be Natural) Growtein Growth Protein Chocolate NET WT. 97 oz. (6 lb) 2750g packaged in plastic bottles - DIETARY SUPPLEMENT; UPC Code: 655455001678, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN - Just Be Natural; INGREDIENTS: Whey protein…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0040-2016·2015-10-28
JBN Cherry Crush Whey Isolate Recalled for Unlabeled Milk Allergen
Nutrition Resource Services, Inc. is recalling JBN Cherry Crush 100% Whey Isolate because the product is not labeled as containing milk.
Product
JBN (Just Be Natural) Cherry Crush 100% WHEY ISOLATE Enhanced Performance Nutrition NET WT. 41.3 oz. (2.58 lb) 1170g - DIETARY SUPPLEMENT; UPC codes: 65545502198, packaged in plastic bottles , MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN -Just Be…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0029-2016·2015-10-28
JBN Chocolate Mocha Whey Protein Recalled for Unlabeled Milk Allergen
Nutrition Resource Services is recalling JBN Chocolate Mocha whey protein powders because they are not labeled as containing milk, a major allergen.
Product
JBN (Just Be Natural) Chocolate Mocha Confidence Nutritional Support for Bariatric Surgery 25G 100% WHEY ISOLATE NET WT. 43.9 oz. (2.7 lb) 1,230g and NET WT. 17.4 oz. (1.1 lb) 492g packaged in plastic bottles- DIETARY SUPPLEMENT; UPC Codes: 655455018294, 655455018195…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0036-2016·2015-10-28
JBN Earth Superior Whey Banana Cream Pie Recalled for Milk Allergen Mislabeling
Nutrition Resource Services is recalling JBN Earth Superior Whey Banana Cream Pie because whey-based protein powders are not labeled as containing milk.
Product
JBN (Just Be Natural) Earth Superior Whey Banana Cream Pie NET WT. 31.5 oz. (1.97 lb) 896g packaged in plastic bottles - DIETARY SUPPLEMENT; UPC code: 65545020136, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN -Just Be Natural INGREDIENTS: Whey…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0053-2016·2015-10-28
JBN Chocolate Truffle Whey Superior Recalled for Unlabeled Milk Allergen
Nutrition Resource Services is recalling JBN Chocolate Truffle Whey Superior because whey-based protein powders are not labeled as containing milk.
Product
JBN (Just Be Natural) Chocolate Truffle Whey Superior NET WT. 30.7 oz. (1.92 lb) 870g - DIETARY SUPPLEMENT; packaged in plastic bottles, UPC code: 655455020525, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN -Just Be Natural INGREDIENTS: Whey protein…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0154-2016·2015-10-28
Berchtold TELETOM Equipment Management System Recall for Control Malfunction
Berchtold Corp. is recalling TELETOM Equipment Management Systems 4 and 6 series due to potential control and brake failure caused by fluid intrusion.
Product
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a ceiling mounted device to supply power, medical gases, and data-communication…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0048-2916·2015-10-28
JBN Creamsicle Recovery Fuel Isolate Recalled for Unlabeled Milk Allergen
Nutrition Resource Services, Inc. is recalling JBN Creamsicle Recovery Fuel ISOLATE because the whey-based product is not labeled as containing milk.
Product
JBN (Just Be Natural) Creamsicle Recovery Fuel ISOLATE, Enhanced Performance Nutrition NET WT. 44.4 oz. (2.8 lb) 1260g - DIETARY SUPPLEMENT, packaged in plastic bottles, UPC code: 655455116976, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN -Just Be…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0156-2016·2015-10-28
Smith & Nephew MOSAICPLASTY Harvesting System Recalled for Packaging Breach
Smith & Nephew is recalling MOSAICPLASTY DP- Disposable Harvesting Systems because a breach in the packaging compromised the device's sterility.
Product
Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile Part Number: 7209235 Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0049-2016·2015-10-28
JBN Chocolate Whey Superior Recalled for Undeclared Milk Allergen
Nutrition Resource Services, Inc. is recalling JBN Chocolate Whey Superior because the product is not labeled as containing milk, a major allergen.
Product
JBN (Just Be Natural) Chocolate Whey Superior NET WT. 29.6 oz. (1.85 lb) 840g and NET WT. 88.9 oz. (5.55 lb) 2,520g - DIETARY SUPPLEMENT, packaged in plastic bottles, UPC codes: 655455020112, 655455001692, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0039-2016·2015-10-28
JBN Growtein Protein Powder Recalled for Unlabeled Milk Allergen
Nutrition Resource Services is recalling JBN Growtein Growth Protein because whey-based products are not labeled as containing milk.
Product
JBN (Just Be Natural) Growtein Growth Protein Vanilla Cream NET WT. 97 oz. (6 lb) 2750g - DIETARY SUPPLEMENT packaged in plastic bottles, UPC code: 655455001661, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN - Just Be Natural; INGREDIENTS: Whey…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0044-2016·2015-10-28
JBN Unflavored Whey Isolate Recalled for Undeclared Milk Allergen
Nutrition Resource Services, Inc. is recalling JBN Unflavored 100% Whey Isolate because the product is not labeled as containing milk, posing a risk to individuals with milk allergies.
Product
JBN (Just Be Natural) Unflavored 100% WHEY ISOLATE Enhanced Performance Nutrition; UPC code: 655455017594, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN -Just Be Natural NET WT. 27.5 oz. (1.72 lb) 780g - DIETARY SUPPLEMENT; packaged in plastic…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0054-2016·2015-10-28
Hospira Recalls Amidate Etomidate Injection Due to Degradation Impurities
Hospira Inc. is recalling 24,100 syringes of Amidate (Etomidate Injection) because stability testing confirmed out-of-specification degradation products.
Product
Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL), LifeShield, 20 mL, Glass Abboject Syringe with male luer lock adapter, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-8060-29
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0143-2016·2015-10-28
ConForMIS iDuo Knee Replacement Recalled for Ethylene Glycol Residue
ConforMIS, Inc. is recalling 12 units of the iDuo Knee Bicompartmental Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConForMIS iDuo Knee Bicompartmental Knee Replacement System , iDUO G2, Right Medial Catalog Number: M57230600220 (US) M5723INT0600220 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0152-2016·2015-10-28
Smiths Medical Recalls Port-A-Cath Needles Due to Incorrect Labeling
Smiths Medical ASD, Inc. is recalling Port-A-Cath Plastic Hub Needles from Lot 46262 because the lid stock labels contain incorrect part numbers, descriptions, and images.
Product
PORT-A-CATH Plastic Hub Needles, 0.9mm (20G) x 19mm (3/4 in.) 90-degree. REF 21-2287-24 The Plastic hub PORT-A-CATH (PAC) needles are intended to access the implantable portal system for the purpose of infusion or withdrawal of fluids. These PAC needles can be used with…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0147-2016·2015-10-28
ConFormis iTotal Knee Replacement System Recalled for Ethylene Glycol Residue
ConforMIS is recalling 110 units of the iTotal Posterior Stabilized Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL PS-IPOLY- IMPLANT KIT-LEFT and ITOTAL PS-IPOLY-IMPLANT KIT-RIGHT Catalog Number:TPS1111111
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0137-2016·2015-10-28
Biomet Thinflap System Cases Recalled Due to Lid Opening Difficulty
Biomet Microfixation is recalling 5 Thinflap System Cases because the lids require excessive force to open.
Product
Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0134-2016·2015-10-28
Synthes Recalls Spinal Pedicle Fixation Rods Due to Finishing Process Error
Synthes (USA) Products LLC is recalling 492 spinal pedicle fixation rods because they were produced using a bead blast process not identified in the manufacturing specification.
Product
5.0mm Unit Rod 270mm, 5.0mm Unit Rod 290mm, 5.0mm Unit Rod 310mm, 5.0mm Unit Rod 330mm, 5.0mm Unit Rod 350mm, 5.0mm Unit Rod 370mm, 5.0mm Unit Rod 390mm, 5.0mm Unit Rod 410mm, 5.0mm Unit Rod 430mm, 5.0mm Unit Rod 450mm; Orthosis, Spinal, Pedicle fixation Intended to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0144-2016·2015-10-28
ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue
ConforMIS, Inc. is recalling 3 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - LEFT ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - RIGHT Catalog Number: TCR1111111
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0035-2016·2015-10-28
JBN Chocolate Whey Protein Powder Recalled for Missing Milk Labeling
Nutrition Resource Services is recalling JBN Chocolate Confidence Nutritional Support for Bariatric Surgery because the whey protein product is not labeled as containing milk.
Product
JBN (Just Be Natural) Chocolate Confidence Nutritional Support for Bariatric Surgery 25G 100% WHEY ISOLATE; NET WT. 43.4 oz. (2.7 lb) 1,230g - packaged in plastic bottles, UPC code: 655455018225, DIETARY SUPPLEMENT MANUFACTURED BY NRS -Nutrition Resource Services, Inc.…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0146-2016·2015-10-28
ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue
ConforMIS, Inc. is recalling 348 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConFormis iTotal CR Knee Replacement System- iTOTAL CR, Right Knee Catalog Number: M57250600020 (US) M5725INT0600020 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0153-2016·2015-10-28
OneTray Sealed Sterilization Containers Recalled for Incorrect Labeling
Innovative Sterilization Technologies LLC is recalling OneTray Sealed Sterilization Containers because the labels list the wrong steam sterilization time.
Product
OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization container used to steam sterilize medical devices
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0149-2016·2015-10-28
Natus neoBLUE 3 Phototherapy System Recalled for Intensity Documentation
Natus Medical is recalling 4,560 neoBLUE 3 Phototherapy systems because the instruction manuals did not accurately reflect the cleared intensity settings.
Product
Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy, Catalogue Part Number: 010066; Top Assembly Part Number: 001103
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0136-2016·2015-10-28
Biomet Neuro Combo Set Case Lid Requiring Excessive Force Recalled
Biomet Microfixation is recalling 37 Neuro Combo Set Cases because the lids require excessive force to open.
Product
Neuro Combo Set Case The cases hold surgical instrumentation in place during handling and storage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0140-2016·2015-10-28
ConForMIS iUNI Knee Replacement Recalled for Ethylene Glycol Residue
ConForMIS is recalling 6 units of the iUNI Unicondylar Knee Replacement System due to potential ethylene glycol residue.
Product
ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2, Right Lateral Catalog Number: M57220600240 (US) M5722INT0600240 (OUS)
Category
Medical Device
Distribution
Distributed nationwide