The Recall Desk

State

Wyoming product recalls

72,940 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.

Which agencies issued them

These figures cover only the 3,219 recalls whose distribution notice names Wyoming 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 76159

  • HighFDA (Food)·H-0379-2026·2026-01-14

    Frozen raw shrimp recalled over possible contamination with Cesium-137

    Direct Source Seafood is recalling 1,800 cases of waterfront BISTRO frozen raw shrimp, sold alongside Market 32 brand shrimp, because the shrimp may be contaminated with Cesium-137.

    Product
    waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB). Product is packaged in white flexible plastic pouch with multicolored labeling. UPC is 0 21130 13224 9. Product of Indonesia. DISTRIBUTED BY LUCERNE FOODS, INC. P.O
    Category
    Food
    Distribution
    17 states
  • HighFDA (Drugs)·D-0251-2026·2026-01-14

    Tri-Moxi intraocular injection recalled over glass-like particulate matter

    Imprimis NJOF is recalling 314 boxes containing 6,280 pre-filled syringes of Tri-Moxi triamcinolone and moxifloxacin intraocular injection over glass-like particles.

    Product
    Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852. NDC 71384-746-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0380-2026·2026-01-14

    Market 32 frozen raw shrimp recalled over possible Cesium-137 contamination

    Direct Source Seafood is recalling 3,290 cases of Market 32 by Price Chopper frozen raw shrimp because the shrimp may be contaminated with Cesium-137.

    Product
    MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel shell on 26/30 count per pound. Net 16oz. Product is packaged in a clear flexible plastic package with brown label and blue and green printing. UPC is 0 41735 01358 3. Product of Indonesia. PROUDLY DISTRIBUTED BY PR
    Category
    Food
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-1037-2026·2026-01-14

    CereLink pressure sensor kits recalled over corrosion stains on the needle

    Integra LifeSciences is recalling 5,116 Codman CereLink ICP Sensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.

    Product
    Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink ICP Sensor Basic Kit consists of the CereLink ICP Sensor (ICP Sensor) and a 14-gauge Tuohy needle with stylet. The ICP Sensor is a nylon tube with a microminiature strain gauge pressure transduc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0255-2026·2026-01-14

    Oxycodone and acetaminophen 7.5 mg tablets recalled over a missing imprint

    SpecGx is recalling 74,544 bottles of Oxycodone and Acetaminophen CII Tablets, 7.5 mg/325 mg, because of the potential for the imprint to be missing on tablets.

    Product
    OXYCODONE AND ACETAMINOPHEN — OXYCODONE AND ACETAMINOPHEN (OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1029-2026·2026-01-14

    Intracranial pressure monitors recalled after customer complaints of rebooting

    Sophysa is recalling 105 Pressio 2 ICP Monitoring Systems following customer complaints of the Pressio monitor rebooting.

    Product
    The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0378-2026·2026-01-14

    Gourmet kunafe pastry recalled because it may contain partially hydrogenated oils

    Ziyad Brothers Importing is recalling 575 cases of Baraka Gourmet Pastry Kunafe because the product may contain partially hydrogenated oils.

    Product
    Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1036-2026·2026-01-14

    Intracranial pressure monitoring kits recalled over corrosion stains on the needle

    Integra LifeSciences is recalling 1,301 Codman Microsensor Basic Kits over potential corrosion stains on the surface of the 14-gauge Tuohy needle included in the kits.

    Product
    Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is required. The kit is indicated for use in both subdural and intraparenchymal pressure monitoring applications only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1026-2026·2026-01-14

    DxI 800 immunoassay analyzers recalled over a failure to restart after shutdown

    Beckman Coulter is recalling 6,457 UniCel DxI 800 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.

    Product
    Beckman Coulter UniCel Dxl 800, Part numbers: 973100, A71456, A71457, A25288; Immunoassay Method, Troponin Subunit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0377-2026·2026-01-14

    French style puff pastry recalled because it may contain partially hydrogenated oils

    Ziyad Brothers Importing is recalling 2,865 cases of Baraka French Style Puff Pastry because the product may contain partially hydrogenated oils.

    Product
    Baraka French Style Puff Pastry 1lb and 1.5lbs sizes, UPCs 8 22514 28540 3 and 8 22514 28550 2, both sizes 12 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1025-2026·2026-01-14

    DxI 600 immunoassay analyzers recalled over a failure to restart after shutdown

    Beckman Coulter is recalling 1,272 UniCel DxI 600 analyzers because a potential communication issue may prevent the instrument restarting after a standard shutdown, causing delayed results.

    Product
    Beckman Coulter UniCel Dxl 600, Part numbers: A71460, A71461, A30260; Immunoassay Method, Troponin Subunit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0254-2026·2026-01-14

    Oxycodone and acetaminophen 10 mg tablets recalled over a missing imprint

    SpecGx is recalling 287,988 bottles of Oxycodone and Acetaminophen CII Tablets, 10 mg/325 mg, because of the potential for the imprint to be missing on tablets.

    Product
    OXYCODONE AND ACETAMINOPHEN — OXYCODONE AND ACETAMINOPHEN (OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26E002000·2026-01-13

    Lippert Recalls 3000 Series Hidden Hinge Ramp Doors for Breakage Risk

    Lippert is recalling 3000 Series Hidden Hinge Ramp Doors because they may break away from the frame during use, increasing the risk of injury.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V006000·2026-01-12

    Terex Recalls 2025 Aerial Devices Due to Hydraulic Overheating Risk

    Terex is recalling 2025 TL, LT, LTM40, HR40, HR46, and SCM55 aerial devices because a control valve defect may cause hydraulic equipment to overheat, posing a burn risk.

    Product
    TEREX — TEREX HR46, LT-SERIES, LTM40, SCM55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V005000·2026-01-09

    Land Rover Recalls 2026 Range Rover Sport for Incorrect Weight Label

    Jaguar Land Rover is recalling 2026 Range Rover Sport vehicles because the certification label lists incorrect weight information, which could lead to overloading.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26172·2026-01-08

    Rattan six-drawer dressers recalled over tip over and entrapment hazards

    About 870 Rattan 6-Drawer Dressers, model YD001, are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.

    Product
    Rattan 6-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26171·2026-01-08

    NFSVLB baby bath seats recalled over tip over and entrapment hazards

    About 1,430 NFSVLB baby bath seats are being recalled because they are unstable, can tip over, and have leg openings that allow a child's torso to become entrapped.

    Product
    NFSVLB Baby Bath Seats (blue)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26169·2026-01-08

    Braided crib bumpers recalled under the federal crib bumper ban

    About 55 SARO Braided Crib Bumpers, Model 1374, are being recalled because they can obstruct an infant's breathing and are banned under the Safe Sleep for Babies Act.

    Product
    SARO Braided Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26181·2026-01-08

    Baby loungers recalled over fall and entrapment hazards to infants

    About 9,300 Joyful Journeys baby loungers are being recalled because the sides are too low, the foot openings are too wide, and the loungers have no stand.

    Product
    Joyful Journeys Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide