The Recall Desk

State

Guam product recalls

72,816 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 72,816 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

126–150 of 73201

  • CriticalFDA (Food)·H-1242-2026·2026-08-26

    Coast Tropical Jalapeno Peppers Recalled for Potential Salmonella Javiana Contamination

    Coast Citrus Distributors is recalling bulk jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed to wholesale distributors and has not been sold at retail.

    Product
    Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes (10lbs, 40lbs, 35lbs, 20lbs, 38lbs 1 1/9 Bushel) ; Product of MX; Coast Tropical TX UPCs 73296608113; 73296600558; 73296610927; 73296600559; 732966107055; 02060042
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0788-2026·2026-08-26

    Fresenius Kabi Recalls Morphine Syringes Due to Labeling Error

    Fresenius Kabi is recalling 625,500 Morphine Sulfate syringes because some were mislabeled and contained Dilaudid instead.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2976-2026·2026-08-26

    Siemens Recalls Emit 2000 Quinidine Assay Due to Precision Issues

    Siemens Healthcare Diagnostics is recalling specific lots of the Emit 2000 Quinidine Assay because unacceptable precision may cause falsely high results, risking improper patient treatment.

    Product
    Beckman Coulter, Emit 2000 Quinidine Assay REF: OSR4Q229 Contents: R1: 2 x 23 mL;R2 2x13 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0801-2026·2026-08-26

    American Regent Recalls Tralement Injection Due to Particulate Matter

    American Regent is recalling 323,000 vials of Tralement (trace elements injection 4) due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    TRALEMENT — TRALEMENT (TRACE ELEMENTS INJECTION 4)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2960-2026·2026-08-26

    Tobii Dynavox Recalls TD Navio Maxi Speech Generating Devices

    Tobii Dynavox is recalling TD Navio Maxi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.

    Product
    TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2975-2026·2026-08-26

    Siemens Quinidine Assay Recalled for Precision Errors

    Siemens is recalling 20 units of the Syva EMIT 2000 Quinidine Assay due to precision issues that may cause inaccurate test results.

    Product
    Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL, 1x14mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0791-2026·2026-08-26

    American Regent Recalls Nitroglycerin Injection Due to Particulate Matter

    American Regent, Inc. is recalling Nitroglycerin injection vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    NITROGLYCERIN — NITROGLYCERIN (NITROGLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2959-2026·2026-08-26

    Tobii Dynavox Recalls TD Navio Midi Speech Generating Devices

    Tobii Dynavox is recalling TD Navio Midi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.

    Product
    TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0793-2026·2026-08-26

    American Regent Recalls Cyanocobalamin Injections Due to Particulate Matter

    American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0794-2026·2026-08-26

    Aminocaproic Acid Injection Recalled for Particulate Matter Contamination

    American Regent, Inc. is recalling Aminocaproic Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    AMINOCAPROIC ACID — AMINOCAPROIC ACID (AMINOCAPROIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0796-2026·2026-08-26

    American Regent Recalls Acetylcysteine Solution Due to Particulate Matter

    American Regent, Inc. is recalling specific lots of Acetylcysteine Solution, USP, 10% due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ACETYLCYSTEINE — ACETYLCYSTEINE (ACETYLCYSTEINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0802-2026·2026-08-26

    FDA Recalls Nicardipine Hydrochloride Injection Due to Particulate Matter

    American Regent, Inc. is recalling 43,460 vials of Nicardipine Hydrochloride Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    NICARDIPINE HYDROCHLORIDE — NICARDIPINE HYDROCHLORIDE (NICARDIPINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0795-2026·2026-08-26

    American Regent Recalls Atropine Sulfate Injection Due to Particulate Matter

    American Regent, Inc. is recalling Atropine Sulfate injection vials because they contain particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ATROPINE SULFATE — ATROPINE SULFATE (ATROPINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0764-2026·2026-08-26

    Shilpa Medicare Recalls Discolored Pemetrexed Injection Vials

    Shilpa Medicare is recalling 18,434 vials of PEMRYDI RTU (pemetrexed injection) due to reports of green to dark green discoloration in the solution.

    Product
    PEMRYDI RTU — PEMRYDI RTU (PEMETREXED DISODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0797-2026·2026-08-26

    American Regent Recalls Acetylcysteine Solution Due to Particulate Matter

    American Regent, Inc. is recalling Acetylcysteine Solution USP due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ACETYLCYSTEINE — ACETYLCYSTEINE (ACETYLCYSTEINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2967-2026·2026-08-26

    Paragonix KidneyVault Portable Renal Perfusion System Recalled for Firmware Defect

    Paragonix Technologies is recalling 1,445 KidneyVault Portable Renal Perfusion Systems because a firmware defect may cause the device to lose configuration, resulting in a blank screen and loss of displayed preservation parameters.

    Product
    Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26E061000·2026-08-26

    Bell Recalls Pit Boss Helmets for Lack of Impact Protection

    Bell Sports is recalling specific Pit Boss helmets that may lack proper impact protection, increasing injury risk in crashes.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2983-2026·2026-08-26

    Fort Defiance Automated Field Steam Sterilizer Recalled for Electrical Grounding Defect

    Fort Defiance Industries is recalling Automated Field Steam Sterilizers because a water recovery system connector may lose ground continuity, creating an unreliable fault current return path.

    Product
    Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2966-2026·2026-08-26

    Siemens Immulite 2000 Syphilis Screen Recalled for Negative Bias

    Siemens Healthineers is recalling Immulite 2000 Syphilis Screen assays because a negative patient bias may cause low reactive results to be reported as nonreactive.

    Product
    Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF(s):L2kSY2/10489085; L2KSY6/10488319 IVD, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2964-2026·2026-08-26

    AVID Medical Recalls Halyard LAVH PACK Due to Sterilization Error

    AVID Medical, Inc. is recalling 40 packs of Halyard LAVH PACK kits because a component was improperly sterilized, potentially causing leaks.

    Product
    Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
    Category
    Medical Device
    Distribution
    Distributed nationwide