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.

3851–3875 of 73325

  • CriticalFDA (Food)·H-0249-2026·2025-12-17

    Infant formula recalled after contamination with Clostridium botulinum

    ByHeart is recalling 3,482,131 cans and 3,531,901 single serve packets of Whole Nutrition Infant Formula after contamination with Clostridium botulinum. The FDA has classified the action as Class I.

    Product
    1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams in packages containing 14 Single Serve Packets
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0902-2026·2025-12-17

    Frozen baby bhindi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen baby bhindi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0222-2026·2025-12-17

    Frozen chopped methi recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen chopped methi after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    NEBIVOLOL — NEBIVOLOL (NEBIVOLOL HYDROCHLORIDE)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0904-2026·2025-12-17

    Frozen mixed vegetables recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen mixed vegetables after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0225-2026·2025-12-17

    Frozen garlic cloves recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen garlic cloves after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0218-2026·2025-12-17

    Frozen jamun recalled after the product tested positive for Salmonella

    Chetak New York is recalling Deep-brand frozen jamun after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    LANTHANUM CARBONATE — LANTHANUM CARBONATE (LANTHANUM CARBONATE)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0892-2026·2025-12-17

    Frozen surti undhiu mix recalled after testing positive for Salmonella

    Chetak New York is recalling Deep-brand frozen surti undhiu mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.

    Product
    Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 7H 38-1008SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 8H; 38-1009SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 9H; 38-1010
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V876000·2025-12-17

    Wheelchair restraint retractors in converted vans may fail to lock

    Rollx Vans is recalling certain converted vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints, because the retractors may not lock and the wheelchair may not be properly secured.

    Product
    HONDA — HONDA, TOYOTA, FORD ODYSSEY, SIENNA, TRANSIT, EXPRESS 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V875000·2025-12-17

    Autocar Recalls 2024 E-ACTT Tractor for Battery Cable Fire Risk

    Autocar is recalling one 2024 E-ACTT terminal tractor because improperly secured battery cable connections may overheat and cause a fire or loss of motive power.

    Product
    AUTOCAR — AUTOCAR E-ACTT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V872000·2025-12-17

    Toyota Highlander third row seat belt anchor may be installed incorrectly

    Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row centre seat belt roof anchor may have been installed at an incorrect angle.

    Product
    TOYOTA — TOYOTA HIGHLANDER HYBRID, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V871000·2025-12-17

    BMW Recalls 2014-2015 Models Due to Head Air Bag Inflator Defect

    BMW is recalling specific 2014-2015 2, 3, and 4 Series vehicles because the head air bag inflator may fail, posing an injury risk during a crash.

    Product
    BMW — BMW M235I, 228I, 328I, 320I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V873000·2025-12-17

    Suzuki Recalls 2025-2026 DR-Z400 Motorcycles for Brake Fluid Leak Risk

    Suzuki is recalling 2025-2026 DR-Z400S and 2025 DR-Z400SM motorcycles because incorrectly tightened screws may allow brake fluid to leak, reducing braking ability.

    Product
    SUZUKI — SUZUKI DR-Z400SM, DR-Z400S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0901-2026·2025-12-17

    Quick Strip plastic bandages recalled over open seals affecting sterility

    Medline is recalling 4,381,400 Quick Strip Plastic Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0887-2026·2025-12-17

    Drainage catheter trays recalled over safety indicators showing the wrong position

    Bard Peripheral Vascular is recalling 1,240 Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator can show the catheter in the sharp position when it is blunt.

    Product
    Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V877000·2025-12-17

    Chrysler Pacifica wheelchair restraints may not lock securely

    Vantage Mobility is recalling 2021–2025 Chrysler Pacifica vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may fail to lock, allowing wheelchairs to move unsecured during transit.

    Product
    HONDA — HONDA, CHRYSLER, TOYOTA ODYSSEY, PACIFICA, SIENNA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V874000·2025-12-17

    Kia Sportage instrument panel screen may fail due to software error

    Kia is recalling certain 2023-2025 Sportage and Sportage Plug-In Hybrid vehicles with a 4.2-inch screen and a Kia tow hitch harness, because a software error may make the instrument panel screen fail.

    Product
    KIA — KIA SPORTAGE, SPORTAGE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0898-2026·2025-12-17

    Fabric bandages recalled over open package seals affecting product sterility

    Medline is recalling 182,526 CURAD Germ-Shield Touch-Free Fabric Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box, Medline Item Number CUR1930F
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Drugs)·D-0226-2026·2025-12-17

    Cinacalcet 90 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 12,576 bottles of Cinacalcet Hydrochloride Tablets, 90 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0900-2026·2025-12-17

    Quick Strip plastic bandages, three quarter inch, recalled over open seals

    Medline is recalling 1,725,600 Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Drugs)·D-0224-2026·2025-12-17

    Cinacalcet 30 mg tablets recalled over a nitrosamine impurity above limits

    Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0903-2026·2025-12-17

    Quick Strip fabric bandages recalled over open seals affecting sterility

    Medline is recalling 6,989,900 Quick Strip Fabric Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.

    Product
    Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25650QS
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0889-2026·2025-12-17

    Immunoassay reaction vessels recalled over manufacturing deformities causing instrument errors

    Beckman Coulter is recalling 38,225 Access 2 Reaction Vessels because certain lots may have a small protrusion or hair-like deformity that can cause instrument errors and delay patient results.

    Product
    Access 2 Reaction Vessels, individual, disposable, plastic tubes used to process patient, quality control and calibration samples on the Access 2 Immunoassay system, Catalog Number 81901
    Category
    Medical Device
    Distribution
    Distributed nationwide