State

Minnesota product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48676–48700 of 81668

HighFDA (Devices)·Z-1774-2017·2017-04-19
Draegar Medical Systems Recalls Kappa and Scio Patient Monitors
Draegar Medical Systems is recalling Kappa and Scio patient monitors because a low oxygen alarm may fail to sound when oxygen levels drop below the set limit.
Product
Kappa, Catalog Number: MS18853 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Catalog Number(s): MS18597/MS18596/MS18853. Product Usage: The devices are intended to be used in the environment where patient care is provided by…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1762-2017·2017-04-19
Merge Healthcare Recalls iConnect Enterprise Archive Software Due to Display Error
Merge Healthcare is recalling iConnect Enterprise Archive software because an error message can prevent users from viewing prior studies. The recall affects 333 sites nationwide and internationally.
Product
iConnect Enterprise Archive (ICEA) software. The firm name on the labeling is Merge Healthcare, Hartland, WI.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1802-2017·2017-04-19
2k Innovations Recalls Heated Neck Garments for Unapproved Medical Claims
2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Neck Garments because FDA inspections found the firm made unapproved therapy and medical claims on product information and its website.
Product
Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0670-2017·2017-04-19
Jubilant Cadista Recalls Bupropion Hydrochloride Tablets Due to Impurities
Jubilant Cadista Pharmaceuticals is recalling Bupropion Hydrochloride Extended-release Tablets because they failed impurity specifications.
Product
BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, packaged in a) 60-count bottles (NDC 59746-316-60) and b) 100-count bottles (NDC 59746-316-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1811-2017·2017-04-19
2k Innovations Recalls Volt Heated Slippers for Unapproved Medical Claims
2k Innovations is recalling Volt Resistance Heated Slippers because FDA inspections found the company made unapproved therapy and medical claims on product information and its website.
Product
Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0655-2017·2017-04-19
FDA Recalls Estradiol Non-Micronized Bulk Due to cGMP Deviations
The FDA is recalling bulk Estradiol Non-Micronized, USP, manufactured by Qinhuangdao Zizhu Pharmaceutical, Co. due to cGMP deviations and lack of quality assurance.
Product
Estradiol Non-Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China
Category
Drug
Distribution
6 states
ModerateFDA (Drugs)·D-0666-2017·2017-04-19
Medisca Recalls Estradiol Bulk Due to cGMP Deviations
Medisca, Inc. is recalling Estradiol, USP Bulk (Hemihydrate) in 25 g and 100 g bottles due to cGMP deviations identified during an FDA inspection.
Product
ESTRADIOL, USP Bulk (Hemihydrate), in a) 25 g (NDC 38779-2261-04) and b) 100 g (NDC 38779-2261-05) bottles, Packed by MEDISCA INC. PLATTSBURGH, NY Product Code 2261
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1804-2017·2017-04-19
2k Innovations Recalls Volt Resistance Heated Therapy Shoulder Wrap
2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Therapy Shoulder Wraps because the firm made unapproved therapy and medical claims on product information and its website.
Product
Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0652-2017·2017-04-19
Citron Pharma Recalls Penicillin V Potassium Tablets Due to Foreign Tablet Presence
Citron Pharma LLC is recalling 420 bottles of Penicillin V Potassium 500 mg tablets because Amoxicillin 500 mg tablets were found in the bottles.
Product
PENICILLIN V POTASSIUM — PENICILLIN V POTASSIUM (PENICILLIN V POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1755-2017·2017-04-19
Zimmer Biomet Recalls MEDTECH ROSA Spine Software Due to Unapproved Change
Zimmer Biomet is recalling MEDTECH ROSA Spine 1.0.2 software because an unapproved change was made by the supplier. The device is used to guide instruments during spine surgery.
Product
MEDTECH ROSA Spine 1.0.2 The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments during spine surgery. Guidance is based on an intra-operative plan developed…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0654-2017·2017-04-19
FDA Recalls Estradiol Micronized Bulk Due to cGMP Deviations
Qinhuangdao Zizhu Pharmaceutical is recalling Estradiol Micronized Bulk for prescription compounding due to cGMP deviations and lack of quality assurance.
Product
Estradiol Micronized Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China (NDC 44132-001-01) (44132-001-06)
Category
Drug
Distribution
6 states
ModerateFDA (Drugs)·D-0668-2017·2017-04-19
McKesson Recalls Hydralazine Hydrochloride Injection Due to Temperature Abuse
McKesson Medical Surgical is recalling 98 vials of Hydralazine Hydrochloride Injection because some were stored refrigerated instead of at room temperature.
Product
HYDRALAZINE HYDROCHLORIDE — HYDRALAZINE HYDROCHLORIDE (HYDRALAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1782-2017·2017-04-19
GE Healthcare Recalls Centricity PACS Web Diagnostic Software
GE Healthcare is recalling 118 units of Centricity PACS Web Diagnostic software due to a defect where study category labels and hanging positions appear incorrectly swapped.
Product
Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources within the system or across computer networks at distributed locations.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0663-2017·2017-04-19
Medisca Recalls Estriol USP Bulk Due to cGMP Deviations
Medisca, Inc. is recalling Estriol, USP (Micronized) Bulk in various bottle sizes due to cGMP deviations identified during an FDA inspection.
Product
ESTRIOL, USP (Micronized) Bulk, in a) 5 grams (NDC 38779-0732-03), b) 25 grams (NDC 38779-0732-04) , c) 100 grams (NDC 38779-0732-05), and d) 1 Kg (NDC 38779-0732-09) bottles, Packed by MEDISCA, INC. PLATTSBURGH, NY 12901; Product Code 0732
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1809-2017·2017-04-19
2k Innovations Recalls Volt Heated Socks for Unapproved Medical Claims
2k Innovations is recalling Volt Resistance Heated Socks because FDA inspections found the product makes unapproved therapy and medical claims.
Product
Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1805-2017·2017-04-19
Volt Resistance Heated Therapy Foot Wrap Recalled for Unapproved Medical Claims
2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Therapy Foot Wraps because FDA inspections found unapproved therapy and medical claims on product information and the company website.
Product
Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1766-2017·2017-04-19
Merit Medical Recalls PreludeSYNC Radial Compression Devices Due to Valve Seal Defect
Merit Medical Systems is recalling 1,940 PreludeSYNC Radial Compression Devices because manufacturing particulates may prevent the inflation valve from sealing completely.
Product
The PreludeSYNC Radial Compression Device is a sterile, single use disposable device used to assist in gaining and maintaining hemostasis of the radial and ulnar artery following catheterization procedures. It has a soft wristband with a secure hook and loop fastener. The band…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0660-2017·2017-04-19
FDA Recalls Levonorgestrel Bulk Drug Due to cGMP Deviations
The FDA is recalling bulk levonorgestrel manufactured by Qinhuangdao Zizhu Pharmaceutical due to cGMP deviations and lack of quality assurance.
Product
Levonorgestrel Non-Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd., Qinhuangdao 066004, China (NDC 44132-012-01),
Category
Drug
Distribution
6 states
ModerateFDA (Drugs)·D-0662-2017·2017-04-19
Signature Club A Recalls Double Hyaluronic 1000 Day Cream for Microbial Contamination
Signature Club A Ltd is recalling 1,237 jars of Double Hyaluronic 1000 Volumizing Day Cream due to microbial contamination.
Product
Double Hyaluronic 1000, 'AN OUNCE OF GOLD' Volumizing Day Cream, Broad Spectrum SPF 30+, (Octinoxate 7.725%, Oxybenzone 6.18%, Octisalate 5.15%, Avobenzone 3.09%), Net Wt. 1.8 oz. (51 g) jar, Distributed by Signature Club A, Ltd, Tampa, FL 33609.
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1803-2017·2017-04-19
FDA Recalls 2k Innovations Heated Lower Back Garment for Unapproved Claims
2k Innovations Inc. is recalling 22,757 Volt Resistance Heated Lower Back Garments because FDA inspections found the firm made unapproved therapy and medical claims on product information and its website.
Product
Volt Resistance Heated Lower Back Garment Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1771-2017·2017-04-19
Cardiovascular Systems Recalls ViperWire Advance Peripheral Guide Wire Due to Sizing Error
Cardiovascular Systems Inc. is recalling one lot of ViperWire Advance Peripheral Guide Wires because they may contain the wrong size product.
Product
ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethylene Oxide. The guide wire is a smooth, stainless steel wire, with a silicone coating, and a radiopaque distal spring tip. The guide wire allows for proper positioning of the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1792-2017·2017-04-19
Windstone Medical Recalls Lasik Trays Due to Sterile Packaging Concerns
Windstone Medical Packaging is recalling 260 Lasik Tray kits because the sterile packaging of the included Medtronic Curity Eye Pad may be compromised.
Product
Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1754-2017·2017-04-19
Zimmer Biomet Recalls 16 MEDTECH ROSA Brain 3.0 Neurosurgical Devices
Zimmer Biomet is recalling 16 MEDTECH ROSA Brain 3.0 neurosurgical devices due to an unapproved change made by the supplier.
Product
MEDTECH ROSA Brain 3.0 The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1808-2017·2017-04-19
2k Innovations Recalls Volt Resistance Frostie Heated Gloves for Unapproved Claims
2k Innovations Inc. is recalling Volt Resistance Frostie Heated Gloves because FDA inspections found the firm made unapproved therapy and medical claims on product information and its website.
Product
Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1807-2017·2017-04-19
2k Innovations Recalls Volt Heated Elbow Garments for Unapproved Claims
2k Innovations is recalling 22,757 Volt Resistance Heated Elbow Garments because FDA inspections found the firm made unapproved therapy and medical claims.
Product
Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps
Category
Medical Device
Distribution
Distributed nationwide