The Recall Desk

State

Guam product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1351–1375 of 73292

  • SevereCPSC·26539·2026-06-11

    Merkury Hot and Cool bladeless fan heaters can overheat and catch fire

    About 18,000 Merkury Innovations Hot + Cool Heating and Cooling Fans are being recalled after two reports of the fan catching fire, one causing smoke damage to property.

    Product
    Hot + Cool Heating and Cooling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V382000·2026-06-11

    International Recalls 2026-2027 HV Trucks for Brake Release Delay

    International is recalling 2026-2027 HV vehicles because the service brake may take longer than expected to release, increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V384000·2026-06-11

    Altec Recalls AC Series Cranes Due to Missing Welds on Jib

    Altec Industries is recalling 2024-2026 AC Series Cranes because missing welds on the 26-foot insulating personnel jib may cause the platform to fall, increasing injury risk.

    Product
    ALTEC — ALTEC AC SERIES CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26550·2026-06-11

    Kawasaki Teryx4 and Teryx5 H2 drive converter sheaves can break

    About 3,585 model year 2026 Kawasaki Teryx4 H2 and Teryx5 H2 off-road vehicles are being recalled after 19 reports of drive converter sheave breakage.

    Product
    Model Year 2026 Teryx4 H2 and Teryx5 H2 recreational off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26536·2026-06-11

    Sloosh dive sticks violate federal ban and pose impalement hazard

    About 254,000 Sloosh dive sticks, sold in packages of Sloosh water toys model 40041, are being recalled because they exceed the compress limit under the federal dive sticks ban.

    Product
    Sloosh Dive Sticks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26555·2026-06-11

    Houoto pool drain covers lack required markings under federal law

    About 595 Houoto 642-2150V pool drain covers are being recalled because they lack required product markings under the Virginia Graeme Baker Pool and Spa Safety Act.

    Product
    Houoto 642-2150V Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2212-2026·2026-06-10

    Pediatric care bed KayserBett IDA recalled due to entrapment hazard

    KayserBett IDA pediatric care beds are being recalled because the hand control can be operated by children, creating a risk of entrapment and serious injury or death.

    Product
    Pediatric care bed; Product Designation: KayserBett IDA;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2248-2026·2026-06-10

    BD Quincke spinal trays recalled over Huons bupivacaine quality issues

    BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2223-2026·2026-06-10

    Ivenix pump software may report false battery health and shut down

    The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.

    Product
    LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2253-2026·2026-06-10

    BD combined Whitacre and Quincke spinal trays recalled over bupivacaine

    BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2278-2026·2026-06-10

    Design Options spinal trays recalled over Huons bupivacaine quality issues

    Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.

    Product
    Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2257-2026·2026-06-10

    BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2252-2026·2026-06-10

    BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2250-2026·2026-06-10

    BD Quincke 26G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
    Category
    Medical Device
    Distribution
    Distributed nationwide