The Recall Desk

State

Iowa product recalls

73,584 recalls have nationwide distribution and so reach Iowa. 5,593 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total
5,593
Critical
910
Severe
1,591
Most recent
2026-10-24

Of the 5,593 recalls naming Iowa we have scored against our rubric, 910 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,591 (28%) are Severe.

Which agencies issued them

These figures cover only the 5,593 recalls whose distribution notice names Iowa specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

926–950 of 79177

  • CriticalFDA (Food)·H-1254-2026·2026-08-26

    Whole Foods Salsa Recalled Due to Potential Salmonella Contamination

    Whole Foods Market is recalling Heirloom Tomato Salsa because it was made with jalapenos that may be contaminated with Salmonella.

    Product
    Whole Foods Salsa, Heirloom Tomato. Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 22860200000, 24091700000, 24118800000…
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Devices)·Z-2978-2026·2026-08-26

    Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus Recall

    Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection System Plus catheters due to a potential for arterial sheath tip separation during use.

    Product
    Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus, Material Number SR-250-NPS; Percutaneous catheter
    Category
    Medical Device
    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-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-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 (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 (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 (Devices)·Z-2872-2026·2026-08-26

    BD Needle Kit for Powered Driver Recall Due to Removal Difficulty

    Bard Access Systems is recalling BD Needle Kits for Powered Drivers because the obturator may lock to the hub, potentially delaying emergency therapy.

    Product
    BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF: D015251NK, BD Needle Kit for Powered Driver 35mm x 15Ga, REF: D015351NK, BD Needle Kit for Powered Driver 45mm x 15Ga, REF: D015451NK, BD Needle Kit for Powered…
    Category
    Medical Device
    Distribution
    32 states
  • 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-2977-2026·2026-08-26

    Boston Scientific ENROUTE Transcarotid Neuroprotection System Recall for Tip Separation

    Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection Systems due to a potential for arterial sheath tip separation or partial tip separation during use.

    Product
    Boston Scientific ENROUTE Transcarotid Neuroprotection System, Material Number SR-200-NPS; Percutaneous catheter
    Category
    Medical Device
    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-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-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 (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-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
  • 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
  • HighFDA (Devices)·Z-2958-2026·2026-08-26

    Arrowhead DE LLC Recalls Arrow-LOK Implants Due to Sterility Assurance Concerns

    Arrowhead DE LLC is recalling 4,171 Arrow-LOK Implants because they did not undergo a required gamma radiation dose audit, which could reduce sterility assurance and lead to patient infection.

    Product
    Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-253535, 21-253540, 21-253545, 21-253550, 21-353513, 21-353516, 27-253519, 27-253522, 27-253525, 27-253528, 27-253530, 27-253533, 27-253535. Implant indicated for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2963-2026·2026-08-26

    Maquet Critical Care Recalls Y Sensor Modules for Electrical Safety Testing Omission

    Maquet Critical Care AB is recalling nine Y Sensor Modules for the SERVO-U/-N ventilator systems because they did not undergo required electrical safety and functional tests during production.

    Product
    GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use. Maquet Critical Care AB, is a subsidiary of Getinge.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2965-2026·2026-08-26

    Siemens Immulite 2000 Syphilis Screen Recall for Negative Bias

    Siemens Healthineers is recalling 24 units of the Immulite 2000 Syphilis Screen assay due to a potential negative patient bias that may report low reactive results as nonreactive.

    Product
    Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF:L2KSY2(D)/10471981 IVD, RxOnly
    Category
    Medical Device
    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