State

Minnesota product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34551–34575 of 81587

SevereFDA (Drugs)·D-0316-2020·2019-11-20
Apotex Recalls Equate Ranitidine Tablets Due to Possible NDMA Contamination
Apotex Inc. is recalling Equate Maximum Strength Ranitidine Tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA). The recall covers 1,132,453 bottles distributed nationwide.
Product
Equate Maximum Strength Ranitidine Tablets, USP 150 mg Acid Reducer 130 Tablets Distributed by Wal-Mart Stores, Inc. Bentonville, AR 72716 a) Twin Pack NDC: 49035-100-07; b) Single Pack NDC: 49035-100-00
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0329-2020·2019-11-20
Viatrexx-Ithurts Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling Viatrexx-Ithurts sterile multi-dose vials because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Ithurts, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0290, NDC 73069-270-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0334-2020·2019-11-20
Viatrexx-Infla Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling Viatrexx-Infla vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide and in Puerto Rico.
Product
Viatrexx-Infla, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0279, NDC 73069-249-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0335-2020·2019-11-20
Viatrexx-Collagen Recalled for Lack of Sterility Assurance
Viatrexx Bio Incorporated is recalling Viatrexx-Collagen vials because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Collagen, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0085, NDC 73069-095-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0342-2020·2019-11-20
Viatrexx-Relief + Sterile Vials Recalled Due to Sterility Assurance Concerns
Viatrexx Bio Incorporated is recalling Viatrexx-Relief + sterile vials because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Relief +, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0615, NDC 73069-450-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0353-2020·2019-11-20
Heritage Medical 2000 Vascular Beds Recalled for Sudden Head Drop Hazard
Heritage Medical Products is recalling 167 2000 Vascular beds due to a potential for the head of the bed to drop suddenly while a patient is lying on it.
Product
2000 Vascular with 30 Degree option
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0341-2020·2019-11-20
Viatrexx-Immunexx Recalled Due to Lack of Sterility Assurance
Viatrexx Bio Incorporated is recalling 18 vials of Viatrexx-Immunexx because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Immunexx, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0270, NDC 73069-244-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0347-2020·2019-11-20
Viatrexx-Male+ Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling Viatrexx-Male+ sterile vials because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Male+, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0400, NDC 73069-320-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0326-2020·2019-11-20
Viatrexx-Connectissue Recalled Due to Lack of Sterility Assurance
Viatrexx Bio Incorporated is recalling Viatrexx-Connectissue vials because they were manufactured in a manner that cannot guarantee sterility.
Product
Viatrexx-Connectissue, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0090, NDC 73069-100-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0317-2020·2019-11-20
Rite Aid Ranitidine Tablets Recalled for Possible NDMA Contamination
Apotex Inc. is recalling Rite Aid Pharmacy Maximum Strength Ranitidine Tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA).
Product
Rite Aid Pharmacy Maximum Strength Ranitidine Tablets, USP 150 mg Cool Mint Acid Reducer 24 Tablets Sugar Free NDC 11822-6107-4 Distributed By: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0348-2020·2019-11-20
Viatrexx-ANS/CNS Recalled for Lack of Sterility Assurance
Viatrexx Bio Incorporated is recalling Viatrexx-ANS/CNS vials because they were manufactured in a manner that cannot guarantee sterility.
Product
Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0025, NDC 73069-039-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0340-2020·2019-11-20
Viatrexx-Arthros Recalled Due to Lack of Sterility Assurance
Viatrexx-Arthros is being recalled because it was manufactured in a manner that cannot guarantee sterility. The product is distributed to physicians nationwide.
Product
Viatrexx-Arthros, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0030, NDC 73069-035-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0314-2020·2019-11-20
Apotex Recalls Walgreens Wal-Zan 150 Tablets Due to NDMA Contamination Risk
Apotex Inc. is recalling Walgreens Maximum Strength Wal-Zan 150 tablets due to possible contamination with the impurity N-nitrosodimethylamine (NDMA).
Product
Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets, USP 150 mg/Acid Reducer Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015 a) 200 Tablets NDC 0363-1030-07; b) 24 Tablets NDC 0363-1030-02; c) 95 Tablets NDC 0363-1030-09; d) 65 Tablets NDC 0363-1030-06
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0345-2020·2019-11-20
Viatrexx-Hair Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling Viatrexx-Hair sterile multi-dose vials because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0251, NDC 73069-206-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0327-2020·2019-11-20
Viatrexx-MuSkel-Neural Recalled Due to Lack of Sterility Assurance
Viatrexx Bio Incorporated is recalling Viatrexx-MuSkel-Neural vials because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-MuSkel-Neural, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC4020, NDC 73069-347-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0310-2020·2019-11-20
Novitium Pharma Recalls Ranitidine Capsules Due to NDMA Impurity
Novitium Pharma LLC is recalling 19,560 bottles of Ranitidine Capsules 150 mg nationwide because the product contains the NDMA impurity.
Product
Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Manufactured by: Novitium Pharma LLC 70 Lake Drive, East Windsor, New Jersey 08520 NDC 70954-001-20
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0333-2020·2019-11-20
Viatrexx-Neuro 3 Recalled Due to Lack of Sterility Assurance
Viatrexx Bio Incorporated is recalling Viatrexx-Neuro 3 vials because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Neuro 3, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0463, NDC 73069-373-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0336-2020·2019-11-20
Viatrexx-Prolo Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling 42 vials of Viatrexx-Prolo because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Prolo, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0558, NDC 73069-443-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0309-2020·2019-11-20
Lannett Recalls Ranitidine Syrup Due to NDMA Impurity
Lannett Company, Inc. is recalling 683,149 bottles of Ranitidine Syrup nationwide because NDMA impurity was detected.
Product
Lannett Ranitidine Syrup (Ranitidine Oral Solution, USP), 15mg/mL Rx Only Distributed by: Lannett Company, Inc. Philadelphia, PA 19154 NDC 54838-550-80
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0328-2020·2019-11-20
Viatrexx-Ouch Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling 19 vials of Viatrexx-Ouch because the manufacturing process cannot guarantee sterility.
Product
Viatrexx-Ouch, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0500, NDC 73069-402-41.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V835000·2019-11-20
Isuzu and Chevrolet Trucks Recalled for Rear Wheel Lug Nut Defect
Isuzu is recalling certain 2017-2020 Isuzu and Chevrolet trucks because rear outer wheel lug nuts may not have been properly tightened, increasing crash risk.
Product
ISUZU — ISUZU, CHEVROLET NPR HD, NPR XD, NQR, NRR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0339-2020·2019-11-20
Viatrexx-GI Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling Viatrexx-GI sterile multi-dose vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide and in Puerto Rico.
Product
Viatrexx-GI, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0211, NDC 73069-189-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0346-2020·2019-11-20
Viatrexx-Neuro Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling Viatrexx-Neuro vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide.
Product
Viatrexx-Neuro, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0460, NDC 73069-375-41.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0338-2020·2019-11-20
Viatrexx-Mesenchyme Recalled Due to Lack of Assurance of Sterility
Viatrexx Bio Incorporated is recalling Viatrexx-Mesenchyme vials because the manufacturing process cannot guarantee sterility. The product was distributed to physicians nationwide.
Product
Viatrexx-Mesenchyme, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0092, NDC 73069-102-41.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0343-2020·2019-11-20
Viatrexx-Intra-Cell Recalled Due to Lack of Sterility Assurance
Viatrexx Bio Incorporated is recalling Viatrexx-Intra-Cell vials because they were manufactured in a manner that cannot guarantee sterility.
Product
Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0280, NDC 73069-250-41.
Category
Drug
Distribution
Distributed nationwide