State

Minnesota product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42001–42025 of 81657

SevereFDA (Food)·F-1626-2018·2018-07-11
Caito Foods Recalls Mixed Melon Products Due to Salmonella Risk
Caito Foods Service, Inc. is recalling multiple brands of mixed melon products due to potential Salmonella contamination. The recall covers products distributed across 23 states.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Caito Foods Disribution MELON MIX 6/10Z, 10 oz., UPC: 81851301331 Clear Generic Label Distributed by Caito Foods Caito Foods Disribution…
Category
Food
Distribution
23 states
SevereFDA (Devices)·Z-2356-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead and Stylet Damage
FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.
Product
microTargeting" Drive System Distributed by Medtronic, Product Number 9033G0601
Category
Medical Device
Distribution
46 states
SevereFDA (Drugs)·D-0891-2018·2018-07-11
Ingenus Recalls Irinotecan Hydrochloride Injection Due to Potency Issues
Ingenus Pharmaceuticals is recalling Irinotecan Hydrochloride Injection because of high out-of-specification assay values for potency.
Product
IRINOTECAN HYDROCHLORIDE — IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1631-2018·2018-07-11
Caito Foods Recalls Mixed Melon Products Due to Salmonella Risk
Caito Foods Service, Inc. is recalling multiple brands of mixed melon products due to potential Salmonella contamination. The products were distributed in 23 states.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Kroger FRUIT MEDLEY 1/10Z, 10 oz., UPC: 826766140176, Clear Generic Label Distributed by Renaissance Food Group Kroger FRUIT MEDLEY 1/24Z…
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1627-2018·2018-07-11
Caito Foods Recalls Kroger Fruit Trays for Salmonella Risk
Caito Foods Service, Inc. is recalling specific Kroger fruit trays with dip due to potential Salmonella contamination. The products were distributed in 23 states.
Product
Kroger FRUIT TRAY SM W/DIP 1/26.75Z, 26.75 oz., UPC: 826766145386 Clear Generic Label Distributed by Renaissance Food Group Kroger FRUIT TRAY LRG W/DIP 1/63Z, 63 oz., UPC: 826766145393 Clear Generic Label Distributed by Renaissance Food Group
Category
Food
Distribution
23 states
SevereFDA (Drugs)·D-0911-2018·2018-07-11
Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error
Fagron Compounding Services is recalling 390 prefilled syringes of Neostigmine Methylsulfate Injection Solution because some may be incorrectly labeled with the wrong strength.
Product
Neostigmine Methylsulfate Injection Solution, 3 mg per 3 mL, 1 mg per mL, 3 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0910-2018·2018-07-11
Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error
Fagron Sterile Services is recalling 840 prefilled syringes of Neostigmine Methylsulfate Injection Solution because they may be incorrectly labeled with the wrong strength.
Product
Neostigmine Methylsulfate Injection Solution, 5 mg per 5 mL, 1 mg per mL, 5 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2345-2018·2018-07-11
FHC microTargeting Drive System Recalled for Lead Damage Risk
FHC, Inc. is recalling 2,952 microTargeting Drive Systems because over-tightening the depth stop screw can damage implanted leads, requiring replacement.
Product
microTargeting" Drive System, Product Number MT-DS
Category
Medical Device
Distribution
46 states
SevereFDA (Food)·F-1647-2018·2018-07-11
Caito Foods Recalls Mixed Melon Products for Salmonella Risk
Caito Foods Service, Inc. is recalling mixed melon products, including Whole Foods Market brand, due to potential Salmonella contamination.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Whole Foods/ Amazon Melon Combo 20 oz., UPC: 826766811205, Whole Foods Market label
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1629-2018·2018-07-11
Caito Foods Recalls Mixed Melon Products Due to Salmonella Risk
Caito Foods Service, Inc. is recalling mixed melon products, including Kroger Salad Fiesta Fruit, due to potential Salmonella contamination.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Kroger SALAD FIESTA FRUIT 1/18Z, 18 oz., UPC: 826766185641 Clear Generic Label Distributed by Renaissance Food Group
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1623-2018·2018-07-11
Caito Foods Recalls Watermelon Products Due to Salmonella Risk
Caito Foods Service, Inc. is recalling various watermelon products due to potential Salmonella contamination. The products were distributed across 23 states.
Product
WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386; WATERMELON SPEAR 6/16Z, 16 oz., UPC: 81851301591; WATERMELON SPEAR 4/28Z, 28 oz.; UPC: 81851301607; WATERMELON CHUNKS 1/5LB, 80 oz., UPC: 81851302147; WATERMELON TRAY 1/5LB, 80 oz., UPC: 81851302239; WATERMELON CHUNK 4/18Z, 18…
Category
Food
Distribution
23 states
SevereFDA (Devices)·Z-2293-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2358-2018·2018-07-11
FHC Depth Stop Adapter Recall Due to Lead Damage Risk
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring surgical replacement.
Product
microTargeting" STar" Drive System (Motorized) Distributed by Medtronic, Product Number FC8002
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2355-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.
Product
microTargeting" Drive System Distributed by Medtronic, Product Number FC1006
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2354-2018·2018-07-11
FHC Depth Stop Adapter Recall for Potential Lead Damage
FHC, Inc. is recalling microTargeting Lead Adapters because over-tightening the depth stop screw can damage implanted leads, requiring replacement.
Product
microTargeting" Lead Adapter for STar" Drive, Product Number 70-CN-DB
Category
Medical Device
Distribution
46 states
SevereNHTSA·18V463000·2018-07-11
Pierce Emergency Vehicles Recalled for Aerial Bracket Detachment Risk
Pierce is recalling 2007-2017 emergency vehicles because an aerial device bracket may detach and fall, potentially striking a person below.
Product
PIERCE — PIERCE IMPEL, ENFORCER, ARROW XT, VELOCITY
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0890-2018·2018-07-11
Ingenus Recalls Irinotecan Hydrochloride Injection Due to Potency Issues
Ingenus Pharmaceuticals is recalling specific lots of Irinotecan Hydrochloride Injection because they had high out-of-specification assay values for potency.
Product
IRINOTECAN HYDROCHLORIDE — IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1625-2018·2018-07-11
Caito Foods Recalls Honeydew and Cantaloupe for Salmonella Risk
Caito Foods Service, Inc. is recalling honeydew and cantaloupe products due to potential Salmonella contamination. The recall covers approximately 3.16 million pounds distributed across 23 states.
Product
Honeydew, Clear Generic Label Distributed by Caito Foods; distributed at Gordon Food Service, Clear Generic Label Distributed by Caito Foods Distributed at Kroger with Clear Generic Label Distributed by Renaissance Food Group Distributed at SpartanNash Distribution…
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1628-2018·2018-07-11
Caito Foods Recalls Multiple Brands of Mixed Melon for Salmonella Risk
Caito Foods Service, Inc. is recalling mixed melon products sold under various brands due to potential Salmonella contamination.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Caito Foods Disribution FRUIT SNACK TRAY 3/32Z, 32 oz., UPC: 81851301454 Clear Generic Label Distributed by Caito Foods Caito Foods…
Category
Food
Distribution
23 states
SevereFDA (Devices)·Z-2351-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage the implanted lead, requiring removal and replacement.
Product
microTargeting" STar" Drive System (Manual), Product Number 70-ZD-MA
Category
Medical Device
Distribution
46 states
SevereNHTSA·18V461000·2018-07-11
Lamborghini Recalls 2015-2016 Aventador Models for Wheel Detachment Risk
Lamborghini is recalling 2015-2016 Aventador SV vehicles because loose brake disc bolts may cause wheels to detach, increasing crash risk.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR, AVENTADOR ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1642-2018·2018-07-11
Caito Foods Recalls Mixed Melon Products for Salmonella Risk
Caito Foods Service, Inc. is recalling multiple brands of mixed melon products due to potential Salmonella contamination. The recall affects approximately 3.16 million pounds of product distributed across 23 states.
Product
Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Walmart SALAD SEASONAL FRUIT 4/10Z 13 oz., UPC: 826766254262 Freshness Guaranteed label
Category
Food
Distribution
23 states
HighFDA (Devices)·Z-2342-2018·2018-07-11
Beaver Visitec Safety Sideport Knife Blades May Detach During Surgery
Beaver Visitec is recalling Safety Sideport Knives because blades may fall out of handles due to non-cured epoxy. The defect poses a risk during ophthalmic surgery.
Product
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V464000·2018-07-11
Volkswagen Recalls 2015-2018 Golf Models for Ignition Key Removal Defect
Volkswagen is recalling 2015-2018 Golf and Golf Sportwagen vehicles because silicate buildup may allow the key to be removed while the car is not in Park, increasing rollaway risk.
Product
VOLKSWAGEN — VOLKSWAGEN GOLF, GOLF SPORTWAGEN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation Complaints
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to higher-than-expected complaints of femoral head/hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-136
Category
Medical Device
Distribution
Distributed nationwide