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Use caution Medical device recall · FDA · Published March 27, 2024

Cardinal Health Jackson-Pratt 3-Spring Reservoir Kit Recall: Unsterilized Products Risk

Cardinal Health recalls specific Jackson-Pratt 3-Spring Reservoir kits shipped without proper sterilization. Affected units have lot numbers 231251D1, 231151D1, 210751D1. Consumers should stop using these kits to prevent infection risks.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1735-2024Medical deviceCardinal Health ›
Take action

Contact the company

Recalling firmCardinal Health 200, LLC3651 Birchwood Dr · Waukegan, IL 60085-8337
✎ GovInfoNow plain-language explainer

Cardinal Health is recalling certain Jackson-Pratt 3-Spring Reservoir kits that were shipped without proper sterilization. Using these kits could lead to infection risks if they are not sterilized before use. Read more at govinfonow.com/recall/55697-cardinal-health-jackson-pratt-3-spring-reservoir-kit-recall-unsterilized.

Source Summary by GovInfoNow · govinfonow.com/recall/55697-cardinal-health-jackson-pratt-3-spring-reservoir-kit-recall-unsterilized · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1735-2024

Cite this page

“Cardinal Health Jackson-Pratt 3-Spring Reservoir Kit Recall: Unsterilized Products Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/55697-cardinal-health-jackson-pratt-3-spring-reservoir-kit-recall-unsterilized. Based on FDA recall #Z-1735-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1735-2024%22&limit=1).

Cardinal Health 200, LLC recalled Jackson-Pratt 3-Spring Reservoir Kits with PVC Round Drain due to products being shipped before sterilization, the FDA said on March 27, 2024.

How to tell if you have it

  • Brand: Cardinal Health
  • Product: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 7Fr., REF SU130-401D
  • Lot Numbers: 231251D1, 231151D1, 210751D1

The hazard

The recall involves specific products shipped to users before undergoing sterilization.

Context

GovInfoNow's records show Cardinal Health 200, LLC has 58 other recalls on record since 2017-06-27. Other recent recalls of similar products include Arrow Paracentesis Kit Recall (2026-04-21), Arrow Peritoneal Lavage Cath Kit Recall (2026-04-21), and Medline Convenience Kits Recall (2026-01-07).

How to tell if you have this one

Check the lot numbers on the kit: 231251D1, 231151D1, or 210751D1. The product includes a PVC round drain, 400mL capacity, and model REF SU130-401D.

  • Brand
    Cardinal Health
  • Category
    Medical device
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Worldwide distribution - US Nationwide and the countries of Panama, Guatemala, Chile, Caribbean Island, Costa Rica.
Recall numberProduct, codes & lotsQuantity
Z-1735-2024Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 7Fr., REF SU130-401D; UDI/DI 50192253016411 (Case), 20192253016410 (Box), 10192253016413 (Each), Lot Numbers: 231251D1, 231151D1, 210751D1202 cases of 12
Z-1736-2024Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 10Fr., REF SU130-402D; UDI/DI 50192253016428 (Case), 20192253016427 (Box), 10192253016420 (Each), Lot Numbers: 231251D2, 231252D2, 231253D2, 231254D2, 231255D2, 231256D2, 231151D2, 231152D2, 231153D2, 210751D2, 210752D2, 210753D2, 210754D2, 210755D22905 cases of 12
Z-1737-2024Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 15Fr., REF SU130-403D; UDI/DI 50192253016435 (Case), 20192253016434 (Box), 10192253016437 (Each), Lot Numbers: 210751D3128 cases of 12
Z-1738-2024Jackson-Pratt Universal Connector PVC Tubing Anti Reflux Transparent Y, REF SU130-4601; UDI/DI 50192253016459 (Case), 10192253016451 (Each), Lot Numbers: 210751D664 cases of 6
Z-1739-2024Jackson-Pratt 3-Spring Reservoir with Silicone Adapters, 400mL, REF SU130-475; UDI/DI 50885380113114 (Case), 10885380113116 (Each), Lot Numbers: 231251D598 cases of 12
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Kit

    Immediately stop using the recalled Jackson-Pratt 3-Spring Reservoir kits with the specified lot numbers to prevent infection risks.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Panama, Guatemala, Chile, Caribbean Island, Costa Rica.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: Mar 27, 202412. FDA classified it Class II: May 1, 202423. Published in FDA’s Enforcement Report: May 8, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Cardinal Health 200, LLC recalls Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive,
March 2, 2026Cardinal Health 200, LLC recalls Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack, REF 1188100777
September 25, 2024

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Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1735-2024 (March 27, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1735-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA