State

Minnesota product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41851–41875 of 81657

HighFDA (Devices)·Z-2479-2018·2018-07-25
Hitachi Oasis MRI Systems Recalled for Exposed Belt Hazard
Hitachi Medical Systems America Inc is recalling 264 Oasis MRI systems because an exposed stainless steel belt can cause finger cuts.
Product
Hitachi Oasis MRI system Product Usage: Hitachi MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The Oasis system produces transverse…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0944-2018·2018-07-25
Avella Recalls Fentanyl and Bupivacaine Cassettes Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 15 cassettes of fentanyl and bupivacaine due to potential bag leakage and lack of sterility assurance.
Product
fentaNYL 3 mcg/mL, 0.1% Bupivacaine, Fentanyl Citrate, USP 750 mcg, Bupivacaine HCL PF, USP, 250 mg, 0.9% Sodium Chloride, USP QS 250 mL. Volume: 250mL. Single dose Cassette. For: Methodist St. John Hospital, By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2467-2018·2018-07-25
GE Medical Systems Recalls T2100 Microflex Drive Treadmill Units
GE Medical Systems is recalling T2100 Microflex Drive Treadmills because unaddressed spare parts may cause uncontrolled walking belt motion during stress tests.
Product
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Specifically the T210…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2464-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling 372 units of Proline Suture Blue 18" 7-0 because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Product
PROLENE SUTURE BLUE 18" 7-0 D/A BV-1, DC631
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2462-2018·2018-07-25
Ethicon Recalls Certain Prolene Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing risks of soft tissue injury or infection.
Product
PROLENE SUTURE 36"(90CM) 3-0 BLU, D9844
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2457-2018·2018-07-25
Ethicon Recalls Prolene Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Prolene suture units because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Product
PROLENE SUTURE 24"(60CM) 6-0 BLUE, D8688
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2316-2018·2018-07-25
Wescam MX-10 Surveillance Laser System Recalled for Ocular Hazard
Wescam Inc is recalling 29 MX-10 surveillance laser systems because the ocular hazard distance is longer than specified, posing a risk of eye exposure.
Product
MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2448-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Proline suture products because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Product
PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C, D10031
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2437-2018·2018-07-25
Siemens Dimension Vista MULTI 1 SDIL Diluent Recall for Defective Septum
Siemens is recalling 197 units of Dimension Vista MULTI 1 SDIL diluent due to a potential defect in the vial cap septum that may cause inaccurate test results.
Product
Dimension Vista¿ MULTI 1 SDIL, KD693, SMN# 10469971
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2447-2018·2018-07-25
NewDeal TIBIAXYS Medical Device Recalled Due to Infection Risk
NewDeal SA is recalling TIBIAXYS devices because use may cause superficial or deep infections requiring antibiotic treatment or device removal.
Product
TIBIAXYS, Model Numbers: 150010S, 150020S, 150030S, 150040S, 150120S, 150110S, 150130S, 150200S, 150240S, 150242S, 150246S, 150250S, 150255S, 150260S, 150265S, 150270S, 150275S, 150280S, 150285S, 150290S, 150514S & 150516S
Category
Medical Device
Distribution
19 states
HighFDA (Food)·F-1651-2018·2018-07-25
TR Toppers Chopped Chocolate Pretzel Pieces Recalled for Peanut Contamination
T R Toppers, Inc. is recalling Chopped Chocolate Pretzel Pieces due to potential peanut contamination. Consumers should check for Lot 10481 and stop using the product.
Product
TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075 GTIN 0 06 51844 10599 6, 7.5 Lbs. (3 x 2.5 Lbs. Bags), Best Kept Between 34¿F and 40¿F <50% Relative Humidity
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2456-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling 300 units of Proline Suture 30" 6-0 Blue because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.
Product
PROLENE SUTURE 30"(75CM) 6-0 BLUE, D8647
Category
Medical Device
Distribution
25 states
ModerateFDA (Devices)·Z-2439-2018·2018-07-25
Opgen Recalls AdvanDx QuickFISH Slides Due to Diminished Performance
Opgen Inc is recalling AdvanDx QuickFISH Slides because they may show diminished performance before their expiration date.
Product
AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012 Control slides included as a component of the QFFIXBC1-25. The slides will provide non-fluorescent, wettable surface with dimensions appropriate for testing…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2480-2018·2018-07-25
Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Product
Presource PBDS, Kit, Common Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0920-2018·2018-07-25
Hain Celestial Recalls alba BOTANICA Sunscreen Due to Incorrect Formulation
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
Product
alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged in a) 4 tubes per case; b) 8 pack shipper display; Manufactured By: The Hain Celestial Group, Inc., Lake Success, NY 11042, UPC 7 24742 01102 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2496-2018·2018-07-25
Philips Ingenuity Digital PET/CT System Recall for Pallet Assembly Defect
Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.
Product
Ingenuity Digital PET/CT System, Model 882446 with the following UDI's: (01)00884838059559(21)900004 (01)00884838059559(21)900005 (01)00884838059559(21)900006 (01)00884838059559(21)900007 (01)00884838059559(21)900008 (01)00884838059559(21)900009…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2482-2018·2018-07-25
Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches
Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Product
Presource PBDS, Kit, No Spiro. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2484-2018·2018-07-25
Stryker Recalls Reprocessed Harmonic Ace Shears Due to Error Code
Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.
Product
Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage: The Reprocessed HARMONIC ACE¿+7, 5 mm Diameter Shears with Advanced Hemostasis are indicated for soft tissue incisions when bleeding control and minimal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2436-2018·2018-07-25
Siemens Dimension Vista CTNI Sample Diluent Recalled for Defective Cap Septum
Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.
Product
Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205
Category
Medical Device
Distribution
53 states
ModerateFDA (Devices)·Z-2430-2018·2018-07-25
Valeris Medical Recalls Apollo XT Suture Anchors Due to Material Mislabeling
Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.
Product
Apollo XT Suture Anchor, 5.5 x 15 Product Usage: Apollo XT Suture Anchors are intended for: Shoulder - Rotator Cuff Repair - Bankart Repair - SLAP Lesion Repair - Biceps Tenodesis - Acromio-Clavicular Separation Repair - Deltoid Repair - Capisular Shift or Capsulolabral…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2468-2018·2018-07-25
Fx Solutions Proton Beam Therapy Heads Recalled for Blister Breach
Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.
Product
Fx SOLUTIONS CENTERED HEAD CoCr 50x19, REF 106-5019 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2483-2018·2018-07-25
Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Product
Presource PBDS, Kit, No Spiro Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2469-2018·2018-07-25
Fx Solutions Offset Heads Recalled for Blister Breach
Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.
Product
Fx SOLUTIONS OFFSET HEAD CoCr 50x20, REF 106-5000 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2442-2018·2018-07-25
Health Harmony Mobile App Recalled for Data Synchronization Delays
Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.
Product
Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a communication tool to display medical device data from third party devices for patients to view, and to collect assessment (question & answers) from…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2438-2018·2018-07-25
Siemens Dimension Vista MULTI 2 SDIL Diluent Recall for Defective Septum
Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.
Product
Dimension Vista¿ MULTI 2 SDIL, KD694, SMN# 10483586
Category
Medical Device
Distribution
53 states