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.

57551–57575 of 81684

ModerateFDA (Drugs)·D-0033-2016·2015-10-21
Ohm Laboratories Recalls Loratadine Tablets for Out-of-Specification Assay
Ohm Laboratories is recalling Premier Value Loratadine Orally Disintegrating Tablets because an assay test result was out of specification.
Product
Premier Value Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box; Distributed by Chain Drug Consortium, 3301 NW Boca Raton Blvd. Suite 101, Boca Raton, FL 33431, NDC 68016-527-31, UPC 8 4098601899 2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0117-2016·2015-10-21
Natus Neurology Recalls NicoletOne Software Due to Signal Obstruction
Natus Neurology is recalling NicoletOne Software v5.94 because a persistent impedance check signal obscures EEG data, potentially affecting clinical monitoring.
Product
NicoletOne Software v5.94, Catalog/Part Number: 482-649600. The NicoletOne data acquisition and review system, either with or without synchronous digital video. The system is intended for medical purposes to record, measure, store and display full band (FbEEG) cerebral EEG and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0029-2016·2015-10-21
Ohm Recalls HEB Loratadine Tablets Due to Out-of-Specification Assay
Ohm Laboratories is recalling HEB Loratadine Orally Disintegrating Tablets because an out-of-specification assay result indicated the drug was superpotent.
Product
HEB Loratadine Orally Disintegrating Tablets, USP, 10 mg, 10-count tablets per box, Made with pride & care for HEB, San Antonio, TX 78204, Item code: 188330, UPC 0 4122081968 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0011-2016·2015-10-21
Boehringer Ingelheim Roxane Recalls Furosemide Tablets Due to CGMP Deviations
Boehringer Ingelheim Roxane Inc. is recalling furosemide tablets USP because the wrong active pharmaceutical ingredient was used during manufacturing.
Product
FUROSEMIDE — FUROSEMIDE (FUROSEMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0015-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Apple Mango, due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Apple Mango, 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-0014-2016·2015-10-21
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-0014-2016·2015-10-21
Actavis Recalls Metformin Hydrochloride Extended-Release Tablets for Dissolution Failure
Actavis is recalling 13,284 bottles of Metformin Hydrochloride Extended-Release Tablets, 1000 mg, because they failed dissolution specifications at the 8-hour timepoint.
Product
Metformin Hydrochloride Extended-Release Tablets, 1000 mg, 60-count bottle, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA; NDC 0591-2720-60; UPC 3 05912 72060 3.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0019-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Organic Apple, due to the potential presence of mold.
Product
GoGo SQueeZ Applesauce, Organic 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 (Food)·F-0022-2016·2015-10-21
Materne Recalls GoGo SQueeZ Applesauce Due to Potential Mold Presence
Materne North America is voluntarily recalling GoGo SQueeZ Applesauce, Berry Pear, due to the potential presence of mold. Consumers should check their pantries for affected lots.
Product
GoGo SQueeZ Applesauce, Berry 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-0015-2016·2015-10-21
Ferring Recalls Bravelle 75 IU Vials Due to Subpotent Drug
Ferring Pharmaceuticals is recalling 32,341 vials of Bravelle 75 IU because the drug was found to be subpotent. The recall is voluntary and nationwide.
Product
Bravelle 75 IU (urofollitropin for injection, purified) For Subcutaneous or Intramuscular Injection Only, 1 Carton (contains 5 single dose vials of Bravelle, 5 single dose vials of 0.9% Sodium Chloride Inj., USP, 2 mL, and 5 Q-Cap Vial Adaptors) , Rx Only, Manufactured for…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0022-2016·2015-10-21
Loratadine Tablets Recalled for Out-of-Specification Assay Results
Ohm Laboratories is recalling CareOne Loratadine tablets because they failed potency testing. Consumers should stop using the affected products.
Product
CareOne Original Prescription Strength, Allergy Relief, Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box, NDC 41520-525-69, UPC 3 41520 31346 2; b) Children's 10-count tablets per box NDC 41520-527-69, UPC 3 41520 31455 1; Distributed…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0035-2016·2015-10-21
TopCare Loratadine Tablets Recalled for Out-of-Specification Assay Results
Ohm Laboratories is recalling TopCare Loratadine tablets because they failed potency testing. Consumers should stop using the affected products.
Product
TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS, , USP, 10 mg, packaged in a) Children's 10-count tablets per box (NDC 36800-528-69, UPC 0 3680010261 3); and b) 10-count tablets per box, (NDC 36800-527-69, UPC 0 3680008395 0); Distributed by Topco Associates, LLC, Elk Grove…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0023-2016·2015-10-21
CVS Loratadine Tablets Recalled for Out-of-Specification Assay Results
CVS Pharmacy loratadine tablets are being recalled because they failed potency testing. Consumers should stop using the product and return it to the pharmacy.
Product
CVS Pharmacy, Original Prescription Strength, LORATADINE ORALLY DISINTEGRATING TABLETS, USP, 10 mg, packaged in a) 10-count tablets per box, Item 876239, UPC 0 50428 61152 4, and b) 30-count tablets per box, Item 367404, UPC 0 50428 11367 7, Distributed by: CVS Pharmacy, Inc.…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0026-2016·2015-10-21
Fred's Loratadine Tablets Recalled for Out-of-Specification Assay Results
Ohm Laboratories is recalling Fred's Loratadine Orally Disintegrating Tablets due to an out-of-specification assay result. The FDA classifies this as a Class III recall.
Product
Fred's Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-counts tablets per box, Distributed by: fred's, Inc., 4300 New Getwell Road, Memphis, TN 38118, UPC 0 8457912198 4.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0037-2016·2015-10-21
Sunmark Loratadine Tablets Recalled for Out-of-Specification Assay Results
Ohm Laboratories is recalling Sunmark loratadine tablets because they failed potency testing. Consumers should stop using the affected products.
Product
Sunmark loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 49348-930-01, UPC 0 1093936544 6); and b) 30-count tablets per box (NDC 49348-930-44, UPC 0 1093934944 6) Distributed by McKesson, One Post Street, San Francisco, CA…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0016-2016·2015-10-21
Tribute Pharmaceuticals Recalls Fenofibric Acid Tablets Due to Benzophenone Contamination
Tribute Pharmaceuticals is recalling specific lots of Fenofibric Acid Tablets because they may contain trace amounts of benzophenone from label varnish.
Product
Fenofibric Acid Tablets, 35 mg, 30-count bottles, labeled as a) FIBRICOR (fenofibric acid) Tablets, NDC 13310-101-07, UPC 3 13310-101-07 8, Manufactured for: AR SCIENTIFIC, INC., Philadelphia, PA 19124 USA; by: MUTUAL PHARMACEUTICAL CO., INC., Philadelphia, PA 19124 USA; b)…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0020-2016·2015-10-21
Rite Aid Loratadine Tablets Recalled for Out-of-Specification Assay
Ohm Laboratories is recalling Rite Aid Pharmacy loratadine orally disintegrating tablets because they failed an assay test, resulting in a superpotent drug classification.
Product
Rite Aid Pharmacy loratadine orally disintegrating tablets USP, 10 mg, packaged in a) 30-count tablets per box, Item 352712, UPC 0 11822 52712 5; b) 60-count tablets per box, Item 353672, UPC 0 11822 53672 1. Distributed By: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0017-2016·2015-10-21
Tribute Pharmaceuticals Recalls Fenofibric Acid Tablets Due to Benzophenone Contamination
Tribute Pharmaceuticals is recalling 140,607 bottles of Fenofibric Acid Tablets 105 mg because they may contain trace amounts of benzophenone from label varnish.
Product
Fenofibric Acid Tablets 105 mg, Rx only, labeled as a) FIBRICOR (fenofibric acid) Tablets, 30-count bottles, NDC 13310-102-07, UPC 3 13310-102-07 5; b) FIBRICOR (fenofibric acid) Tablets, 90-count bottles, NDC 13310-102-90, UPC 3 13310-102-90 7; Manufactured for: AR SCIENTIFIC…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0031-2016·2015-10-21
Major Loratadine Tablets Recalled for Out-of-Specification Assay Results
Ohm Laboratories is recalling Major loratadine orally disintegrating tablets due to out-of-specification assay results. The recall covers 29,360 boxes distributed nationwide.
Product
Major loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets per box, Distributed by Major Pharmaceuticals 31778 Enterprise Drive, Livonia, MI 48150, USA, NDC 0904-5806-15, UPC 3 0904580615 9
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0021-2016·2015-10-21
Ohm Laboratories Recalls Loratadine Tablets Due to Assay Failure
Ohm Laboratories is recalling specific batches of loratadine tablets because they failed potency testing. Consumers should stop using the affected products.
Product
Health Best Choice Care, Loratadine Orally Disintegrating Tablets, USP, 10 mg, 10-count tablets per box, Proudly Distributed by: Valu Merchandisers, Co., Kansas City, MO 64111; UPC 0 7003861209 4
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0038-2016·2015-10-21
Ohm Laboratories Recalls Loratadine Tablets Due to Potency Issues
Ohm Laboratories is recalling Wal-itin Loratadine Orally Disintegrating Tablets because they failed potency testing. The FDA classified this as a Class III recall.
Product
Wal-itin Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-coiunt tablets per box, (NDC 0363-0527-69, ITEM 367492,UPC 3 1191717021 3); and b) 30-count tablets per box, (NDC 0363-0527-31, ITEM 254166, UPC 3 191715562 ) Distributed by Walgreen Co., 200 Wilmot…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0034-2016·2015-10-21
Safeway Care Loratadine Tablets Recalled for Out-of-Specification Assay
Ohm Laboratories is recalling Safeway Care Loratadine Orally Disintegrating Tablets because they failed potency testing. Consumers should stop using the affected products.
Product
Safeway Care Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 21130-527-69, UPC 3 2113076240 9); b) 30-count tablets per box (NDC 21130-527-31, UPC 3 2113076252 2) Distributed by Safeway Inc. PO BOX 99, Pleasanton, CA 94566
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V682000·2015-10-20
Volvo Recalls 2016 VN Trucks for Transmission Locking Hazard
Volvo is recalling 2016 VN trucks because the manual transmission may lock or cause the vehicle to move unexpectedly, increasing crash risk.
Product
VOLVO — VOLVO VN
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·16013·2015-10-20
API Outdoors Recalls Climbing Tree Stands Due to Fall Hazard
Global Manufacturing Company is recalling API Outdoors climbing tree stands because the cable assembly can release, posing a fall hazard.
Product
Climbing tree stands
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·15E085000·2015-10-20
Cummins Westport ISL G Engine Recall for Turbocharger Oil Leak Risk
Cummins is recalling Westport ISL G engines due to a turbocharger oil supply line that may leak, increasing the risk of fire near the exhaust manifold.
Product
ENGINE AND ENGINE COOLING:ENGINE:OTHER FUEL TYPES:TURBO/SUPERCHARGER recall
Category
Vehicle
Distribution
Distributed nationwide