The Recall Desk

State

Minnesota product recalls

72,940 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,804
Critical
1,125
Severe
1,892
Most recent
2026-09-09

Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3726–3750 of 80744

  • HighFDA (Devices)·Z-1079-2026·2026-01-21

    Azurion interventional systems recalled over nine identified software issues

    Philips Medical Systems Nederland is recalling 990 Azurion R3.0 systems over nine identified software issues, including loss of X-ray after a pedal tap and continuous restart.

    Product
    Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0401-2026·2026-01-21

    SMV BodyTrack nuclear medicine systems recalled over a potential detector fall

    GE HealthCare is recalling 12 units of the SMV BodyTrack nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.

    Product
    Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1101-2026·2026-01-21

    Spinal tray syringes recalled over a crack on the syringe collar

    ICU Medical is recalling 64,290 Portex Spinal Trays because syringes may have a crack on the collar, which may lead to delayed or repeated blood draws and blood leakage.

    Product
    Portex Spinal Tray, Item No. A3729-24 A3595
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V026000·2026-01-21

    Keystone Recalls Travel Trailers Due to Ramp Door Breakage Risk

    Keystone RV Company is recalling 2024-2026 Fuzion, Raptor, Redwood, and Voltage travel trailers because the ramp door may break away from the frame, increasing injury risk.

    Product
    KEYSTONE — KEYSTONE VOLTAGE, REDWOOD, RAPTOR, FUZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1018-2026·2026-01-21

    MRI systems recalled over ice that may block magnet venting

    Canon Medical Systems is recalling 22 Vantage Titan 3T MRI systems because ice in the magnet venting system could lead to a helium vessel rupture during a quench.

    Product
    VANTAGE TITAN 3T Model MRT-3010/MEXL-3010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1051-2026·2026-01-21

    Pre-op kits recalled because they contain recalled B. Braun administration sets

    Medline is recalling 32 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1075-2026·2026-01-21

    Allura Xper FD20, model 722028, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 2 Allura Xper FD20 systems because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD20; Model Number: 722028;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1061-2026·2026-01-21

    Hydrophilic catheters recalled over an incorrect expiration date on labeling

    Hangzhou Bever Medical Devices is recalling 149,310 BD Ready-to-Use Hydrophilic Catheters, 14 Fr, over a labeling error giving an incorrect expiration date.

    Product
    BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1056-2026·2026-01-21

    IV start kits recalled over recalled B. Braun administration sets inside

    Medline is recalling 5314 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1053-2026·2026-01-21

    Donor nephrectomy accessory kits recalled over recalled B. Braun sets

    Medline is recalling 33 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1077-2026·2026-01-21

    Allura Xper FD20/20 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD20/20; Model Number: 722038;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1060-2026·2026-01-21

    Allura Xper FD10 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 56 units of the Allura Xper FD10, model 722010, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-PLASTIC CRANIOFACIAL PK-LF, Medline kit SKU DYNJ0395085V; 2) NH PERI DISC PACK, Medline kit SKU DYNJ66311C; 3) DISCECTOMY PACK, Medline kit SKU DYNJ86770; 4) TOTAL KNEE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1091-2026·2026-01-21

    Azurion systems recalled over six identified software issues

    Philips Medical Systems Nederland is recalling 10,466 Azurion systems on software versions R2.1.10 and R2.2.10 over six identified software issues including continuous restart.

    Product
    Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Numbers: 722063, 722221. 2. Azurion 3 M15. Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12. Model Num
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1059-2026·2026-01-21

    Neuro angio packs recalled over recalled B. Braun administration sets inside

    Medline is recalling 12 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1073-2026·2026-01-21

    Allura Xper FD20 Biplane, model 722013, recalled over a missing drip tray

    Philips Medical Systems Nederland is recalling 23 units of the Allura Xper FD20 Biplane, model 722013, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10; Model Number: 722026;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0280-2026·2026-01-21

    PALACOS MV plus G bone cement recalled because ampoules may not break

    Heraeus Medical is recalling PALACOS MV+G pro 40 and PALACOS MV+G pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.

    Product
    Swan, White Clear Alcohol, 50%, 16oz, 12 count
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1062-2026·2026-01-21

    Allura Xper FD10C systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 38 Allura Xper FD10C systems because the drip tray beneath the cooling unit may not have been installed.

    Product
    Product Name: Allura Xper FD10C; Model number: 722001;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0256-2026·2026-01-21

    Fluocinolone topical solution recalled after failing an impurity specification

    Sun Pharmaceutical Industries is recalling 24,624 bottles of Fluocinolone Acetonide Topical Solution 0.01% after an out of specification result for a known impurity.

    Product
    FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0259-2026·2026-01-21

    Carotid anesthesia kits recalled over recalled B. Braun administration sets inside

    Medline is recalling 10 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1063-2026·2026-01-21

    Allura Xper FD10F systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 12 units of the Allura Xper FD10F, model 722002, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD10F; Model Number: 722002;
    Category
    Medical Device
    Distribution
    Distributed nationwide