The Recall Desk

State

Wyoming product recalls

72,907 recalls have nationwide distribution and so reach Wyoming. 3,219 additional recalls listed Wyoming specifically in their distribution scope.

What the numbers show

Total
3,219
Critical
762
Severe
543
Most recent
2026-09-02

Of the 3,219 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 543 (17%) are Severe.

These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

526–550 of 76126

  • HighFDA (Devices)·Z-2810-2026·2026-08-05

    Arterial Cannula Recalled Due to Risk of Pinhole Leaks During Bypass

    Medtronic is recalling 3,621 EOPA 3D Arterial Cannula DIL TIP 22FR units because pinhole leaks may occur during cardiopulmonary bypass, risking hypovolemia, vessel injury, hypotension, ischemia, and organ dysfunction.

    Product
    EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78222
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2805-2026·2026-08-05

    Permobil Recalls M5 Corpus Power Wheelchairs Due to Firmware Drive Inhibit Issue

    Permobil Inc. is recalling 715 M5 Corpus Power Wheelchairs (REF 120032) because firmware versions 1.27 through 1.57 lack drive inhibit logic, which may allow driving under restricted conditions and cause instability.

    Product
    M5 Corpus Power Wheelchair REF,120032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1190-2026·2026-08-05

    Mellish Island Super Skin Dietary Supplement Recalled Over Undeclared Fish Collagen

    Mellish Island Corp. is recalling 1,600 bottles of Super Skin dietary supplement because the label does not declare that its marine collagen comes from fish, a potential allergen.

    Product
    Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2826-2026·2026-08-05

    Blood Analyzer Bar Code Reader May Assign Patient Results to Incorrect Patient ID

    Instrumentation Laboratory is recalling certain GEM Premier 5000 blood analyzer systems because the bar code reader wand may assign patient results to the wrong patient ID.

    Product
    Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number: 00024019255 Portable blood analyzer system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2801-2026·2026-08-05

    Neurological Sponges Recalled Due to Potential Variability in Endotoxin Levels

    Medicom is recalling specific lots of Ritmed Neurological Sponges (Models 55992C to 55998C) because of potential unexpected variability in endotoxin levels.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Neuro Pack, Pack Number AMS12195C; 2) Neuro Pack, Pack Number AMS12195D; 3) Neuro Pack, Pack Number AMS12307; 4) Neuro Spine Pack, Pack Number AMS16313; 5) Lami Kukkar Pack, Pack Number AMS17958; 6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2820-2026·2026-08-05

    OsteoBallast and Ballast bone graft extenders recalled due to insufficient material volume

    IsoTis OrthoBiologics, Inc. is recalling OsteoBallast and Ballast bone graft extenders because they may contain less demineralized bone matrix than intended.

    Product
    OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2812-2026·2026-08-05

    Medical Convenience Kits Recalled Due to Supplier Quality Issue with Lidocaine Injection

    Windstone Medical Packaging is recalling 15 AMS spinal convenience kits, lot 230451, because they contain Elevaris Lidocaine HCl injection recalled for supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL KIT, Part Number AMS13683A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2813-2026·2026-08-05

    AMS Medical Convenience Kits Recalled Due to Supplier Quality Issues

    Windstone Medical Packaging is recalling specific AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr Fred Chiu Single Shot Epi Tray - Rx, Part Number AMS1095(E ; 2) Single Shot Epidural Tray - RX, Part Number AMS11296A; 3) Nerve Block Tray - RX, Part Number AMS11314A; 4) Epidural Tray - RX, Part Nu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2817-2026·2026-08-05

    Medical Convenience Kits Containing Lidocaine Injection Recalled Due to Supplier Quality Issues

    Windstone Medical Packaging is recalling 100 AMS convenience kits labeled Block Tray - RX, Part Number AMS12414, because they contain Elevaris Lidocaine HCl injection recalled for supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Block Tray - RX, Part Number AMS12414
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2815-2026·2026-08-05

    Medical Convenience Kits Containing Lidocaine Injection Recalled Due to Supplier Quality Issues

    Windstone Medical Packaging is recalling 60 AMS Angio Pack-RX convenience kits (lots 230658, 231173) because the included Elevaris Lidocaine HCl injection was recalled by its manufacturer due to supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio Pack - RX, Part Number AMS9461
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0731-2026·2026-08-05

    Azelaic Acid Gel 15% Recalled Over Grainy, Gritty, or Sandy Texture

    Glenmark Pharmaceuticals is recalling azelaic acid gel 15% after receiving complaints that the product felt grainy, gritty, or sandy. The nationwide recall covers specific lots with expiration dates from February through April 2028.

    Product
    AZELAIC ACID — AZELAIC ACID (AZELAIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2814-2026·2026-08-05

    AMS Medical Convenience Kits Recalled Due to Supplier Quality Issues

    Windstone Medical Packaging is recalling specific AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Nerve Block Tray - RX, Part Number AMS13975A; 2) Universal Block Tray- RX, Part Number AMS2009; 3) Nerve Block Tray - RX, Part Number AMS3224.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2816-2026·2026-08-05

    Medical Convenience Kits Recalled Due to Lidocaine Supplier Quality Issues

    Windstone Medical Packaging is recalling 24 AMS Heart Cath Tray convenience kits containing Elevaris Lidocaine HCl injection because the lidocaine was recalled for supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Heart Cath Tray - RX, Part Number DDS1159B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2818-2026·2026-08-05

    Medical Convenience Kits Recalled Over Lidocaine Supplier Quality Issue

    Windstone Medical Packaging is recalling 3,378 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP because the lidocaine was recalled due to supplier quality issues.

    Product
    AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Loop Recorder Pack 2 -RX, Part Number AMS10164; 2) NY Tray - RX, Part Number AMS10276A; 3) NYC Tray - RX, Part Number AMS10281B; 4) Vein Pack - RX, Part Number AMS11398C; 5) Radiology Tray-RX, Part N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0738-2026·2026-08-05

    Dabigatran Etexilate Capsules Recalled Due to Impurity Specification Failure

    Ascend Laboratories, LLC is recalling Dabigatran Etexilate Capsules (75 mg) because testing showed impurities exceeded established limits during stability testing.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0739-2026·2026-08-05

    Dabigatran Etexilate Capsules Recalled Over Impurity Specification Failure

    Ascend Laboratories is recalling dabigatran etexilate capsules due to an out-of-specification result in related substance testing involving Impurity II, Impurity III, and total impurities observed during 12-month stability testing.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0737-2026·2026-08-05

    Dabigatran Etexilate Capsules Recalled Due to Impurity Specification Failure

    Ascend Laboratories, LLC is recalling Dabigatran Etexilate Capsules (150 mg) because testing showed impurities exceeded established limits during stability testing.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V505000·2026-08-04

    Escape Recalls 2025-2026 E13 F1 Trailers Due to Carbon Monoxide Risk

    Escape Trailer Industries is recalling 2025-2026 E13 F1 recreational trailers because insufficient refrigerator ventilation may allow carbon monoxide to build up inside the cabin.

    Product
    ESCAPE — ESCAPE ESCAPE 13
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V506000·2026-08-04

    Wabash Recalls 2027 Van Trailers for Unlabeled ABS Indicator Light

    Wabash is recalling 2027 Van Trailers because the external ABS malfunction indicator light may lack a label, potentially confusing other drivers.

    Product
    WABASH — WABASH VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V504000·2026-08-03

    Rosenbauer Recalls Emergency Vehicles with Faulty Display Units

    Rosenbauer is recalling certain 2024-2026 emergency vehicles because a display unit may fail, preventing the activation of exterior lights and firefighting equipment.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL HV507, COMMERCIAL M2-106
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V503000·2026-08-03

    Forest River Recalls 2027 Freelander and Leprechaun RVs for Fire Risk

    Forest River is recalling 2027 Freelander and Leprechaun recreational vehicles because a missing breaker leaves the power feed wire without overcurrent protection, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER FREELANDER, LEPRECHAUN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E052000·2026-08-03

    Daimler Trucks Recalls Aftermarket Grote Headlamps Due to Software Error

    Daimler Trucks North America is recalling aftermarket Grote Headlamps because a software error may cause low beams to illuminate improperly, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V502000·2026-07-31

    Royal Truck Recalls Traffic Control Vehicles Due to Solar Panel Screw Loosening

    Alamo Group is recalling 2022-2026 Royal Truck & Equipment Class 2 Traffic Control trucks because solar panel screws may loosen, causing the panel to detach and strike others.

    Product
    ROYAL TRUCK & EQUIPMENT — ROYAL TRUCK & EQUIPMENT TRAFFIC CONTROL VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide