The Recall Desk

State

Guam product recalls

72,940 recalls have nationwide distribution and so reach Guam. 385 additional recalls listed Guam specifically in their distribution scope.

What the numbers show

Total
385
Critical
14
Severe
37
Most recent
2026-01-28

Of the 385 recalls naming Guam we have scored against our rubric, 14 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 37 (10%) are Severe.

These figures cover only the 385 recalls whose distribution notice names Guam specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4226–4250 of 73325

  • ModerateFDA (Drugs)·D-0164-2026·2025-11-26

    Skin protectant ointment recalled over contamination found at its manufacturing facility

    DermaRite Industries is recalling 2,673 tubes of DermaMed Ointment because it was made at the same facility where other products and lots were found to be contaminated.

    Product
    DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0539-2026·2025-11-26

    Clotting time cartridges recalled over dried blood on carton labels

    Medtronic is recalling 3,850 HR-ACT clotting time cartridges after trace amounts of dry blood were observed on the external carton label and instructions in five boxes.

    Product
    Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0567-2026·2025-11-26

    Micro collection tube extenders recalled over an inadequate quality system

    ASP Global is recalling 27,100 SAFE-T-FILL micro collection tube extenders over an inadequate quality system with unvalidated manufacturing processes.

    Product
    SAFE-T-FILL Micro Collection Tube Extender, Model 09 1004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0562-2026·2025-11-26

    Sodium heparin blood gas tubes recalled over an inadequate quality system

    ASP Global is recalling 160,250 SAFE-T-FILL plastic blood gas capillary tubes, 230 microlitres with sodium heparin, over an inadequate quality system.

    Product
    SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 230 ¿L; Prepared with Sodium Heparin Model/Catalog Number: 06 0009 Product Description: A clear, plastic capillary blood collection tube
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0557-2026·2025-11-26

    Blood gas capillary tubes recalled over an inadequate quality system

    ASP Global is recalling 397,000 SAFE-T-FILL plastic blood gas capillary tubes, 150 microlitres, because they were manufactured under an inadequate quality system with unvalidated processes.

    Product
    SAFE-T-FILL Plastic Blood Gas Capillary Tubes, 150 ¿L; Prepared with Balanced Heparin Model 06 0186 Product Description: A clear, plastic capillary blood collection tube coated with Heparin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0547-2026·2025-11-26

    Clot activator microtubes recalled over an inadequate quality system

    ASP Global is recalling 27,950 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with clot activator, over an inadequate quality system.

    Product
    SAFE-T-FILL Micro Capillary Blood Collection, 200 ¿L; Prepared with Clot Activator; Red Model/Catalog Number: 07 7150 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0566-2026·2025-11-26

    Capillary mixing fleas recalled over an inadequate quality system

    ASP Global is recalling 50,250 mixing fleas for SAFE-T-FILL blood gas capillaries over an inadequate quality system with unvalidated processes.

    Product
    Mixing Fleas for SAFE-T-FILL Blood Gas Capillaries, Model 07 9503
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0161-2026·2025-11-26

    Moisturizing skin cream recalled over contamination found at the manufacturing facility

    DermaRite Industries is recalling DermaCerin Skin Protectant Moisturizing Cream because it was made at the same facility where other products and lots were found to be contaminated.

    Product
    DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%), packaged in a) 106 g (3.75 oz.) per tube (NDC 61924-174-04) and b) 454 g (16 oz.) per jar (NDC 61924-174-16), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0177-2026·2025-11-26

    Antiperspirant spray recalled over contamination found elsewhere at the facility

    DermaRite Industries is recalling 37,379 spray bottles of UltraSure Anti-Perspirant & Deodorant because it was made at the same facility where other products were found contaminated.

    Product
    UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0552-2026·2025-11-26

    Three hundred microlitre heparin tubes recalled over unvalidated manufacturing processes

    ASP Global is recalling 6,050 SAFE-T-FILL micro capillary blood collection tubes, 300 microlitres with lithium heparin, over an inadequate quality system.

    Product
    SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07 7251 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0159-2026·2025-11-26

    Bromocriptine capsules recalled after an out of specification impurity result

    Zydus Pharmaceuticals is recalling 36,624 bottles of Bromocriptine Mesylate Capsules USP 5 mg after an out of specification result for the 2-Bromoergine impurity.

    Product
    BROMOCRIPTINE MESYLATE — BROMOCRIPTINE MESYLATE (BROMOCRIPTINE MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V816000·2025-11-25

    Rivian delivery van driver seat belt pretensioner cable can be damaged

    Rivian is recalling certain 2022-2025 EDV vehicles because the driver's seat belt pretensioner cable may become damaged and fail to restrain the occupant as intended in a crash.

    Product
    RIVIAN — RIVIAN EDV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V817000·2025-11-25

    International truck control units can lose ABS and stability control

    International is recalling certain 2016-2026 trucks with Bendix control units because electrical noise may cause the ECU to misprocess commands or stop working, disabling ABS and stability control.

    Product
    INTERNATIONAL — INTERNATIONAL 7600, RH, MV, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V818000·2025-11-25

    Volvo Recalls XC60 Models Due to Improperly Tightened Front Seat Bolts

    Volvo is recalling 2018, 2025, and 2026 XC60 vehicles because front seat bolts may be loose. This defect could prevent seats from restraining occupants during a crash.

    Product
    VOLVO — VOLVO XC60MHEV, XC60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V819000·2025-11-25

    2026 Cadillac Vistiq Electric Vehicles Missing Owner's Manual

    General Motors is recalling certain 2026 Cadillac Vistiq electric vehicles because the radio may not have been configured to download the electronic owner's manual during production. Without access to the manual, owners may not know how to safely use and operate the vehicle.

    Product
    CADILLAC — CADILLAC VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V815000·2025-11-25

    2026 Chevrolet Silverado 1500, 2500, 3500 Missing Owner Manuals

    General Motors is recalling certain 2026 Chevrolet Silverado 1500, 2500, and 3500 vehicles because some may not have received an owner's manual during production. Without the manual, owners may not know how to safely use child restraint anchorages, increasing crash injury risk.

    Product
    CHEVROLET — CHEVROLET SILVERADO 1500, SILVERADO 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V812000·2025-11-24

    Newell Recalls 2022 P50 Coaches Due to Seat Mounting Defect

    Newell Coach Corp. is recalling 2022 P50 coaches because improperly welded pedestal mounting plates may cause seat assemblies to detach, increasing crash injury risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V813000·2025-11-24

    Foretravel Recalls Realm and Realm 450 Vehicles for Seat Weld Defect

    Foretravel is recalling 2020-2022 Realm and 2022 Realm 450 vehicles because a seat mounting plate may be improperly welded, allowing the seat to detach.

    Product
    FORETRAVEL — FORETRAVEL REALM, REALM 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V814000·2025-11-24

    nuCamp Trailers Recalled for Incorrect Weight Labels

    Pleasant Valley is recalling 2025-2026 nuCamp trailers because incorrect weight information on labels may lead to unintentional overloading and increased crash risk.

    Product
    NUCAMP — NUCAMP TAG, TAB 400, TAB 360, TAB 320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V810000·2025-11-21

    Altec Recalls 2019-2024 AT Series Vehicles Due to Emergency Stop Defect

    Altec is recalling 2019-2024 AT Series vehicles because the lower emergency stop may not function when the upper control is selected, increasing the risk of death or serious injury.

    Product
    ALTEC — ALTEC AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26103·2025-11-20

    Riding lawn mowers recalled after 15 reports of unexpected bouncing

    About 650 model year 2025 Spartan SRT-XD and KGZ-XD riding mowers are being recalled because incorrectly installed steering arm dampers can cause bouncing and loss of control.

    Product
    Model Year 2025 Spartan SRT-XD and KGZ-XD riding lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26096·2025-11-20

    Folding learning towers recalled after 14 reports of the platform collapsing

    About 9,780 Grow 'N Stow Folding Learning Towers are being recalled because the platform inside the tower can collapse; 14 collapses have been reported including one child with bruises.

    Product
    Grow 'N Stow Folding Learning Tower
    Category
    Consumer Product
    Distribution
    Distributed nationwide