State

Minnesota product recalls

73,741 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,849
Critical: 1,137
Severe: 2,245
Most recent: 2026-10-28

Of the 7,849 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 2,245 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40276–40300 of 81590

ModerateFDA (Drugs)·D-0036-2019·2018-10-24
Saline Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Discount Drug Mart and Food Fair Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Discount Drug Mart, Food Fair, Saline Nasal Spray (sodium chloride) 0.65%, packaged as a) 3 FL OZ (89 mL) bottle UPC 0 93351 01833 6; b) 1.5 FL OZ (45 mL) bottle UPC 0 93351 01834 3, Distributed by: Discount Drug Mart, 211 Commerce Drive, Medina, OH 44256
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0172-2019·2018-10-24
Life Technologies Recalls Gibco DPBS Due to Leaky Bottle Caps
Life Technologies is recalling 240 units of Gibco DPBS due to defective bottle caps that compromise sterility.
Product
Gibco DPBS, calcium, magnesium, for In-Vitro Diagnostic Use SKU 14040141
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0032-2019·2018-10-24
CVS Health Sterile Saline Nasal Mist Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling CVS Health Sterile Saline Nasal Mist due to manufacturing deviations that could impact product quality.
Product
CVS Health, Sterile Saline Nasal Mist (sodium chloride) Allergy & Sinus Relief, 3.0%, 4.25 OZ (126 g) can, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 41854 3.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0123-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect
Zimmer Biomet is recalling 24 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the product was opened in surgery.
Product
Affixus Hip Fracture Nail Right 125 9 mm x 260 mm, Item Number 814309260 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0115-2019·2018-10-24
Siemens ADVIA Centaur CKMB Master Curve Material Recalled for Bias
Siemens Healthcare Diagnostics is recalling ADVIA Centaur CKMB Master Curve Material due to a potential bias identified when compared to internal standards.
Product
ADVIA Centaur CKMB Master Curve Material, Cat No. 07867768 Product Usage: For in vitro diagnostic use for evaluating the ADVIA Centaur CKMB assay. This material is intended to be run singly as unknown samples after a two-point calibration has been performed on the system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0146-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 78 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.
Product
Affixus Hip Fracture Nail Left 125 9 mm x 300 mm, Item Number 814409300 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0153-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects
Zimmer Biomet is recalling 68 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and two foreign countries.
Product
Affixus Hip Fracture Nail Left 125 11 mm x 360 mm, Item Number 814411360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0055-2019·2018-10-24
Product Quest Recalls OCEAN Saline Nasal Spray Due to Quality Deviations
Product Quest Manufacturing LLC is recalling OCEAN Saline Nasal Spray bottles nationwide because they were manufactured under conditions that could impact product quality.
Product
OCEAN Saline Nasal Spray, packaged in a) 3.5 Fl. Oz. (104 mL) bottle UPC 3 01875 26001 9; b) 45 cc (1.5 fl. oz.) UPC 3 01875 26003 3, c) Buddy Pack containing one 1.5 FL. OZ. (44 mL) and one 0.76 FL.OZ. (22 mL) bottle per carton, Distributed by: Valeant Consumer Products, A…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0080-2019·2018-10-24
Product Quest Recalls Family Dollar Saline Nasal Spray for Quality Issues
Product Quest Manufacturing LLC is recalling Family Dollar Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Family Dollar Saline Nasal Spray 4.25 oz. can, 24 pk, SKU 0900562.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0121-2019·2018-10-24
CryoLife Pulmonary Hemi-Artery Graft Recalled for Labeling Error
CryoLife, Inc. is recalling one CryoPatch SG Pulmonary Hemi-Artery graft because the conduit and branch lengths were switched on the product labeling.
Product
CryoPatch SG Pulmonary Hemi-Artery, 1 graft
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0078-2019·2018-10-24
Rexall Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Rexall Extra Moisturizing No Drip Nasal Spray due to manufacturing conditions that could impact product quality.
Product
Rexall, Extra Moisturizing No Drip Nasal Spray (Oxymetazoline Hydrochloride 0.05%) 1 FL OZ (30 mL) bottle, 48 pk. (12687901)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0054-2019·2018-10-24
TopCare Saline Nasal Gel Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling TopCare Saline Nasal Gel with Soothing Aloe due to manufacturing conditions that could impact product quality.
Product
TopCare, Saline Nasal Gel with Soothing Aloe, 0.5 OZ (14 g) tube, Distributed By Topco Associates LLC, Elk Grove Village, IL 60007, UPC 0 36800 42146 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0163-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 50 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the products were opened in surgery.
Product
Affixus Hip Fracture Nail Right 130 13 mm x 360 mm, Item Number 814513360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0130-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 20 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the product was opened in surgery.
Product
Affixus Hip Fracture Nail Right 125 9 mm x 460 mm, Item Number 814311460 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0057-2019·2018-10-24
Product Quest Recalls Best Choice Nasal Spray Due to Manufacturing Deviations
Product Quest Manufacturing LLC is recalling Best Choice 12 Hour Sinus Relief Nasal Spray because it was manufactured under conditions that could impact product quality.
Product
Best Choice, 12 Hour Sinus Relief, Nasal Spray (Oxymetazoline Hydrochloride 0.05%) Nasal Decongestant, 1 FL OZ (30 mL) bottle, Proudly Distributed By: Valu Merchandisers, Co,. 5000 Kansas Ave, Kansas City, KS 66106, UPC 0 70038 63684 7.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0044-2019·2018-10-24
FDA Recalls Premier Value Nasal Spray Due to Manufacturing Deviations
Product Quest Manufacturing LLC is recalling Premier Value Nasal Decongestant Extra Moisturizing Nasal Spray because it was manufactured under conditions that could impact product quality.
Product
Premier Value Nasal Decongestant Extra Moisturizing Nasal Spray (Oxymetazoline HCl 0.05%), 1 FL OZ (30 mL) bottle, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca Raton, FL 33431, NDC 68016-304-03, UPC 8 40986 01518 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0165-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 14 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the product was opened in surgery.
Product
Affixus Hip Fracture Nail Left 130 11 mm x 360 mm, Item Number 814611360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0180-2019·2018-10-24
OriGen Biomedical Recalls Reinforced Dual Lumen Cannulas Due to Deficiencies
OriGen Biomedical is recalling 452 units of Reinforced Dual Lumen Cannulas due to missing barium sulfate and incorrect tip length markings.
Product
Reinforced Dual Lumen Cannula, 16Fr., REF: VV16F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0132-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects
Zimmer Biomet is recalling 27 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.
Product
Affixus Hip Fracture Nail Right 125 11 mm x 340 mm, Item Number 814311340 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0194-2019·2018-10-24
Siemens Atellica Analyzer Software Recall for Diagnostic Errors
Siemens is recalling Atellica Solution software version 1.13 and lower due to five behavioral issues that may cause incorrect test results or sample handling errors.
Product
Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0030-2019·2018-10-24
CVS Health Saline Nasal Mist Recalled for Quality Control Issues
Product Quest Manufacturing LLC is recalling CVS Health Sterile Saline Nasal Mist due to manufacturing deviations that could impact product quality.
Product
CVS Health, Sterile Saline Nasal Mist (sodium chloride) Saline Nasal Moisturizer, 0.9%, packaged in a) Net Wt. 1.52 OZ (43 g) can UPC 0 50428 37079 7 Product #896831; b) Net Wt. 4.25 OZ (120 g) can UPC 0 50428 36124 5; c) Children's Net Wt. 2 OZ (57 g) can UPC 0 50428 58685 3…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0022-2019·2018-10-24
Humco Recalls Thyroid USP Powder Due to Inconsistent Active Ingredient Levels
Humco Holding Group, Inc. is recalling specific lots of Thyroid, USP (Porcine) powder because the levels of active ingredients are inconsistent.
Product
Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only 1000 grams NDC 0395-8077-43 Packaged by: Humco Texarkana, TX 75501
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0033-2019·2018-10-24
CVS Health Baby Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling CVS Health Baby Nasal Spray/Drops due to manufacturing conditions that could impact product quality.
Product
CVS Health, Baby Nasal Spray/Drops, Non-Medicated, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 29380 5 Product #459367.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0038-2019·2018-10-24
Product Quest Recalls Saline Nasal Mist Due to Manufacturing Deviations
Product Quest Manufacturing LLC is recalling 46,056 cans of FAMILY wellness Sterile Saline Nasal Mist because they were manufactured under conditions that could impact product quality.
Product
FAMILY wellness, Sterile Saline, Nasal Mist, Saline Nasal Relief (0.9% Sodium Chloride Solution), 4.25 FL OZ (126 mL) can, Distributed by: Midwood Brands, LLC, 10611 Monroe Rd., Matthews, NC 28105, UPC 0 32251 11617 9.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0046-2019·2018-10-24
Premier Value Sterile Saline Nasal Mist Recalled for Quality Concerns
Product Quest Manufacturing LLC is recalling 10,584 cans of Premier Value Sterile Saline Nasal Mist due to manufacturing deviations that could impact product quality.
Product
Premier Value, Sterile Saline Nasal Mist, Saline Nasal Moisturizer (0.9% Sodium Chloride) Solution, 4.25 FL OZ (126 mL) can, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca Raton, FL 33431, NDC 8 40986 02998 1.
Category
Drug
Distribution
Distributed nationwide