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.

Which agencies issued them

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.

3726–3750 of 73325

CriticalFDA (Food)·H-0338-2026·2025-12-31
Pecan cranberry holiday bark recalled over undeclared wheat in 134,865 bags
Silvestri Sweets is recalling 134,865 bags of Choceur Pecan Cranberry & Cinnamon Holiday Bark over undeclared wheat. The FDA has classified the action as Class I.
Product
Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag. 5 oz. (142g). UPC: 4069365095829. Wholesale unit is split case, with 9 of each item per case.
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0933-2026·2025-12-31
Vapor 2000 anesthetic vaporizers recalled over an out of specification component
Draeger is recalling 431 Vapor 2000 anesthetic vaporizers because a certain component was not delivered within specification and contained impurities. The action is Class I.
Product
Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0939-2026·2025-12-31
Ophthalmic surgical packs recalled over incomplete seals affecting sterility
Alcon Research is recalling 151 Custom Pak ophthalmic procedure packs because the packs may have incomplete seals affecting sterility. The FDA has classified the action as Class I.
Product
Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Numbers: 9903-20, 17188-04, 19762-03, 19203-04, 19203-04, 17957-10 Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience k
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0934-2026·2025-12-31
Vapor 3000 anesthetic vaporizers recalled over an out of specification component
Draeger is recalling 188 Vapor 3000 anesthetic vaporizers because a certain component was not delivered within specification and contained impurities. The action is Class I.
Product
Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0339-2026·2025-12-31
Cookie butter holiday bark recalled over undeclared pecan in 134,865 bags
Silvestri Sweets is recalling 134,865 bags of Choceur Cookie Butter Holiday Bark over undeclared pecan. The FDA has classified the action as Class I.
Product
Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz. (142g). UPC: 4069365095690. Wholesale unit is split case, with 9 of each item per case.
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V914000·2025-12-31
Braun Ambulances Recall Emergency Vehicles Due to Battery Isolator Defect
Braun Industries is recalling 2021-2026 emergency vehicles because a battery isolator may fail, causing loss of electrical systems and patient support.
Product
BRAUN AMBULANCES — BRAUN AMBULANCES LIBERTY TYPE I, SELECT CHIEF XL I, EXPRESS PLUS TYPE I, CHIEF XL TYPE III
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0990-2026·2025-12-31
Dialysis concentrate 100230 recalled because safety and efficacy cannot be assured
Diasol is recalling 4,400 gallons of liquid concentrate for bicarbonate dialysis, product 100230-10-DEX100, because the safety and efficacy of the dialysis acid concentrate cannot be assured.
Product
Brand Name: Diasol Product Name: 100230-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0988-2026·2025-12-31
Dialysis concentrate 100125 recalled because safety and efficacy cannot be assured
Diasol is recalling 7,200 gallons of liquid concentrate for bicarbonate dialysis, product 100125-10-DEX100, because the safety and efficacy of the dialysis acid concentrate cannot be assured.
Product
Brand Name: Diasol Product Name: 100125-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0980-2026·2025-12-31
Femoral nails, 420 mm left trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 23 Affixus Antegrade Femoral Nails, model 815609420, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609420 Software Version: N/A Product Description: Affixus 9 mm, Length 420 mm, Left, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0981-2026·2025-12-31
Femoral nails, 440 mm left trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 24 Affixus Antegrade Femoral Nails, model 815609440, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609440 Software Version: N/A Product Description: Affixus 9 mm, Length 440 mm, Left, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0241-2026·2025-12-31
Aprepitant oral suspension kits recalled over potential metal particulates
Merck Sharp & Dohme is recalling 3 single-dose kits of Emend (aprepitant) for oral suspension over the potential presence of metal particulates in the product.
Product
EMEND — EMEND (APREPITANT)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0982-2026·2025-12-31
Femoral nails, 280 mm left piriformis, recalled over undersized shaft diameter
Zimmer is recalling 3 Affixus Antegrade Femoral Nails, model 815809280, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815809280 Software Version: N/A Product Description: Affixus 9 mm, Length 280 mm, Left, Priformis Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0975-2026·2025-12-31
Femoral nails, 320 mm left trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 23 Affixus Antegrade Femoral Nails, model 815609320, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609320 Software Version: N/A Product Description: Affixus 9 mm, Length 320 mm, Left, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0962-2026·2025-12-31
Medication dispensing cabinets recalled after a firmware update caused drawer failures
CareFusion 303 is recalling 53,669 BD Pyxis automated dispensing cabinet units after a drawer firmware update caused a duplicate address error and drawer failure.
Product
BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis Pro 7-Drawer Auxiliary, REF: 1149-00, BD Pyxis Pro 7- Drawer Auxiliary with Secure Tower, REF: 1152-00, BD Pyxis Pro MedStation Main,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0968-2026·2025-12-31
Femoral nails, 340 mm right trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 22 Affixus Antegrade Femoral Nails, model 815509340, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509340 Software Version: N/A Product Description: Affixus 9 mm, Length 340 mm, Right, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0989-2026·2025-12-31
Dialysis concentrate 100220 recalled because safety and efficacy cannot be assured
Diasol is recalling 4400 gallons of liquid concentrate for bicarbonate dialysis, product 100220-10-DEX100, because the safety and efficacy of the dialysis acid concentrate cannot be assured.
Product
Brand Name: Diasol Product Name: 100220-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0977-2026·2025-12-31
Neurostimulator programmer app recalled over a device reset message that persisted
Medtronic Neuromodulation is recalling 7,667 Restore Clinician Programmer Application devices after a Device Reset message could not be cleared, in rare cases preventing therapy from resuming.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609360 Software Version: N/A Product Description: Affixus 9 mm, Length 360 mm, Left, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0973-2026·2025-12-31
Femoral nails, 440 mm right trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 22 Affixus Antegrade Femoral Nails, model 815509440, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509440 Software Version: N/A Product Description: Affixus 9 mm, Length 440 mm, Right, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0996-2026·2025-12-31
Femoral nails, 360 mm left trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 24 Affixus Antegrade Femoral Nails, model 815609360, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET US CT900B PROG CT900B CLINICIAN TABLET EU -UK CT900C PROG CT900C CLINICIAN TABLET UK CT900D PROG CT900D CLINICIAN TABLET GLOBAL CT900E P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0976-2026·2025-12-31
Femoral nails, 340 mm left trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 24 Affixus Antegrade Femoral Nails, model 815609340, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609340 Software Version: N/A Product Description: Affixus 9 mm, Length 340 mm, Left, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0967-2026·2025-12-31
Femoral nails, 320 mm right trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 22 Affixus Antegrade Femoral Nails, model 815509320, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509320 Software Version: N/A Product Description: Affixus 9 mm, Length 320 mm, Right, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0979-2026·2025-12-31
Femoral nails, 400 mm left trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 24 Affixus Antegrade Femoral Nails, model 815609400, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609400 Software Version: N/A Product Description: Affixus 9 mm, Length 400 mm, Left, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0969-2026·2025-12-31
Femoral nails, 360 mm right trochanteric, recalled over undersized shaft diameter
Zimmer is recalling 22 Affixus Antegrade Femoral Nails, model 815509360, because an undersized distal shaft diameter could lead to implant fatigue fracture.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509360 Software Version: N/A Product Description: Affixus 9 mm, Length 360 mm, Right, Trochanteric Nail Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0987-2026·2025-12-31
Dialysis concentrate 100225 recalled because safety and efficacy cannot be assured
Diasol is recalling 186,000 containers of liquid concentrate for bicarbonate dialysis, product 100225-10-DEX100, because the safety and efficacy of the dialysis acid concentrate cannot be assured.
Product
Brand Name: Diasol Product Name: 100225-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0966-2026·2025-12-31
Infusion software recalled over concentration limits with insufficient decimal precision
ICU Medical is recalling LifeShield Drug Library Management software because Concentration Limits can only be defined to one decimal place instead of three, which may result in over- or under-delivery.
Product
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software Suite v2.2 Product No. 17003-02
Category
Medical Device
Distribution
Distributed nationwide