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.

57526–57550 of 81684

HighFDA (Devices)·Z-0123-2016·2015-10-21
Clinical Innovations Recalls Ebb Complete Tamponade System Due to Balloon Leak Risk
Clinical Innovations, LLC is voluntarily recalling the Ebb Complete Tamponade System due to a potential balloon leak that may prevent the device from delivering therapy when needed.
Product
The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY. Intended for use in providing temporary control or reduction of postpartum uterine bleeding.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0020-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Organic Apple Peach, due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Organic Apple Peach, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Drugs)·D-0025-2016·2015-10-21
Ohm Laboratories Recalls Equaline Loratadine Tablets for Assay Failure
Ohm Laboratories is recalling Equaline loratadine tablets because they failed potency testing. Consumers should stop using the product and return it to the pharmacy.
Product
Equaline Original Prescription Strength, loratadine orally disintegrating tablets, USP, 10 mg, packaged in a) 10-count tablets per box, NDC 41163-528-69, UPC 0 4116347138 2; and b) 30-count tablets per box, NDC 41163-528-31, UPC 0 4116346654 8; Distributed by: Supervalu Inc.…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0024-2016·2015-10-21
Ohm Laboratories Recalls Loratadine Tablets Due to Out-of-Specification Assay
Ohm Laboratories is recalling specific lots of loratadine tablets because they failed potency testing. Consumers should stop using the affected medication.
Product
Discount Drug Mart Food Fair, Original Prescription Strength, Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box, Distributed by: Drug Mart-Food Fair, Medina, OH 44256, UPC 0 93351 12101 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0018-2016·2015-10-21
Mentholatum Recalls WellPatch Capsaicin Patches Due to Labeling Error
The Mentholatum Company is recalling WellPatch Capsaicin Pain Relief Patches because the word 'not' was missing from safety instructions, potentially leading to improper use.
Product
WellPatch¿ Capsaicin Pain Relief Patch, 0.025% Natural Capsaicin, External Analgesic, 4 Large Patches, Distributed by Consignor; The Mentholatum Company, Orchard Park, NY, Manufactured by Consignee; Mentholatum (China) Pharmaceuticals, Guangdong China --- NDC 10742-8126-2, UPC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0027-2016·2015-10-21
Good Neighbor Pharmacy Loratadine Tablets Recalled for Potency Issues
Ohm Laboratories is recalling Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets because they failed potency testing.
Product
Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) For kids 10-count tablets per box, NDC 24385-0161-52, ABC # 042-226, UPC 0 8770140650 8; b) For adults 10-count tablets, NDC 46122-0140-52, ABC# 059-535, UPC 0877014065546, Distributed…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0124-2016·2015-10-21
Synthes Humerus Plates Recalled for Incorrect Part Number Labeling
Synthes (USA) Products LLC is recalling 36 units of VA-LCP Humerus Plates because one part number was incorrectly etched on the device.
Product
Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm- Sterile and Synthes 2.7MM/3.5MM VA-LCP Extended Medial Distal Humerus Plates 10H/RT/189mm-Sterile The Synthes 2.7 mm/3.5 mm Variable Angle LCP Elbow System is intended for fixation of fractures of the…
Category
Medical Device
Distribution
19 states
ModerateFDA (Food)·F-0017-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Apple Pear, due to the potential presence of mold. The recall affects 34,573 cases distributed in the US and Canada.
Product
GoGo SQueeZ Applesauce, Apple Pear, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Drugs)·D-0028-2016·2015-10-21
Ohm Laboratories Recalls Loratadine Tablets Due to Potency Issues
Ohm Laboratories is recalling specific batches of loratadine orally disintegrating tablets because they failed potency testing. Consumers should stop using the affected products.
Product
Health Mart Pharmacy loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets per box, Distributed by: McKesson, One Post Street, San Francisco, CA 94104, NDC 62011-0073-1, UPC 0 5256913369 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0032-2016·2015-10-21
Ohm Allergy Relief Loratadine Recalled for Out-of-Specification Assay
Ohm Laboratories is recalling 311 boxes of Allergy Relief (Loratadine) tablets due to an out-of-specification assay result.
Product
ALLERGY RELIEF — ALLERGY RELIEF (LORATADINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0012-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce products due to the potential presence of mold. Consumers should check their pantries for affected lots.
Product
GoGo SQueeZ Applesauce, Apple Apple, individually wrapped in foil pouch in cardboard carton; sizes include: 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Devices)·Z-0127-2016·2015-10-21
Arrow International Recalls PICC Catheters Due to Labeling Inaccuracy
Arrow International Inc is recalling 4FR Single Lumen Pressure Injectable PICC catheters because the instructions state they withstand 10 pressure injections, but they are only tested for 5.
Product
4FR Single Lumen Pressure Injectable PICC; intravascular therapeutic catheter, for long-term use greater than 30 days.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0023-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Apple Strawberry, due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Apple Strawberry, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Food)·F-0013-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Apple Peach Sweet Potato, due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Apple Peach Sweet Potato, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Drugs)·D-0039-2016·2015-10-21
Meijer Loratadine Tablets Recalled for Out-of-Specification Assay
Ohm Laboratories is recalling Meijer Loratadine Orally Disintegrating Tablets due to an out-of-specification assay result.
Product
Meijer Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box, Dist. By Meijer Distribution Inc. 2929 Walker Avenue NW, Grand Rapids, MI 49544. NDC 41250-527-31, UPC 7 6023662291 8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0019-2016·2015-10-21
QC Quality Choice Loratadine Tablets Recalled for Out-of-Specification Assay
Ohm Laboratories is recalling QC Quality Choice Loratadine Orally Disintegrating Tablets due to an out-of-specification assay result.
Product
QC Quality Choice Loratadine Orally Disintegrating Tablets, USP 10 mg, 10-count tablets per box, Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376-0995, NDC 63868-157-10, UPC 6 35515 95777 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0126-2016·2015-10-21
Synthes Screw Inserter Recalled for Incorrect Etched Graphics
Synthes (USA) Products LLC is recalling 793 units of the Screw Inserter because the etched graphics may not correspond to the instrument's actual angle.
Product
Synthes Screw Inserter; for use with Intramedullary Rod, orthopedic device. Used to secure the head element to the head element inserter to prevent disengagement during head element insertion.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0024-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Variety Packs Due to Potential Mold
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce Variety Packs due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Variety Packs, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Drugs)·D-0012-2016·2015-10-21
Boehringer Ingelheim Roxane Recalls Furosemide Tablets Due to Manufacturing Error
Boehringer Ingelheim Roxane Inc. is recalling 5,160 bottles of Furosemide Tablets USP because the wrong active ingredient was used during manufacturing.
Product
FUROSEMIDE — FUROSEMIDE (FUROSEMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0021-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Apple Pumpkin Cinnamon, due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Apple Pumpkin Cinnamon, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Drugs)·D-0030-2016·2015-10-21
Ohm Recalls Loratadine Tablets Due to Out-of-Specification Assay Results
Ohm Laboratories is recalling specific batches of Leader Loratadine Orally Disintegrating Tablets because they failed potency testing. Consumers should stop using the affected products.
Product
Leader Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box, Distributed by Cardinal Health, Dublin, OH 43017, NDC 37205-745-65, UPC 0 9629512322 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0018-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Apple Grape, due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Apple Grape, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Drugs)·D-0036-2016·2015-10-21
Ohm Recalls Up&Up Loratadine Tablets for Out-of-Specification Assay
Ohm Laboratories is recalling Up&Up loratadine tablets because they failed an assay test, potentially making them superpotent.
Product
Up&Up loratadine orally disintegrating tablets, USP, 10 mg, 30-count tablets per box, Distributed by Target Corp, Minneapolis, MN 55403; NDC 11673-527-31, UPC 3 5166052731 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0016-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Apple Banana, due to the potential presence of mold. The recall affects 34,573 cases distributed in the US and Canada.
Product
GoGo SQueeZ Applesauce, Apple Banana, individually wrapped in foil pouch in cardboard carton; sizes include 4-pack, 12-pack, 16 pack, 18-pack, 20-pack, or 48-pack
Category
Food
Distribution
30 states
ModerateFDA (Devices)·Z-0122-2016·2015-10-21
Alere Cholestech LDX Multianalyte Controls Recalled for Incorrect Ranges
Alere San Diego is recalling Cholestech LDX Multianalyte Controls because the assigned control ranges for Total Cholesterol and Triglycerides are incorrect.
Product
Alere Cholestech LDX Multianalyte Controls, PN 88769 and 88773. Enables users to monitor the performance of total cholesterol (TC), high density lipoprotein cholesterol (HDL), triglycerides (TRG) and glucose (GLU) test procedures.
Category
Medical Device
Distribution
Distributed nationwide