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Lower risk Medical device recall · FDA · Published February 1, 2023

BD Ultra-Fine Insulin Syringes Recall: Nonsterile Risk of Infection

Becton Dickinson recalls BD Ultra-Fine Insulin Syringes (0.5mL, 8mm, 31G) due to nonsterile condition potentially causing infections. Affected lots expire by 2027.

🇺🇸 FDA recall #Z-1240-2023Medical deviceBecton Dickinson ›
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Recalling firmBecton Dickinson & Company1 Becton Dr · Franklin Lakes, NJ 07417-1815
✎ GovInfoNow plain-language explainer

What happened, in plain English

Becton Dickinson is recalling insulin syringes that may not be sterile, increasing infection risk. This affects people using insulin for diabetes who own the specific lots listed. Read more at govinfonow.com/recall/58970-bd-ultra-fine-insulin-syringes-recall-nonsterile-risk-of-infection.

Source Summary by GovInfoNow · govinfonow.com/recall/58970-bd-ultra-fine-insulin-syringes-recall-nonsterile-risk-of-infection · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1240-2023

Cite this page

“BD Ultra-Fine Insulin Syringes Recall: Nonsterile Risk of Infection.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58970-bd-ultra-fine-insulin-syringes-recall-nonsterile-risk-of-infection. Based on FDA recall #Z-1240-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1240-2023%22&limit=1).

Why it’s dangerous

The syringes may not be sterile, which can expose patients to harmful bacteria. This could lead to infections at the injection site, especially in people with diabetes who need frequent injections.

Who’s affected

People using insulin for diabetes who own the recalled syringes (0.5mL, 8mm, 31G) are affected. Those with diabetes who use these syringes are at higher risk of infection.

How to tell if you have this one

Check for the lot numbers: 2038580 (expiring May 2027), 2063298 (expiring May 2027), or 2137904 (expiring July 2027). The syringes are 0.5mL, 8mm, 31G for insulin use.

  • Brand
    Becton Dickinson
  • Category
    Medical device
FDA recall event · 8 products

All 8 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 Chile, Colombia, Dominican Republic, Bahamas, Panama, Peru, Mexico, El Salvador, Mexico, Malaysia, Philippines, Vietnam, Hong Kong, Taiwan, Thailand, Canada.
Recall numberProduct, codes & lotsQuantity
Z-1237-2023BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326679; UDI_DI: N/A Lot Number: 2164338 Exp Date: 2027083145, 000 units
Z-1238-2023BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml, 12.7mm, 28G Single Unit Scale. Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329420; GTIN: (01) 00382903294206 Lot Number: 2038204 Exp. Date: 20270430961,000 units
Z-1239-2023BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml, 12. 7mm, 28G Two Unit Scale- Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329424; GTIN : (01) 00382903294244 Lot Number: 2024074 Exp. Date: 2024074; Lot Number: 2045195 Exp. Date: 202704301,921,000 units
Z-1240-2023BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326713; GTIN: N/A Lot Number: 2038580, Exp. Date: 20270531; Lot Number: 2063298, Exp. Date: 20270531; Lot Number: 2137904, Exp. Date: 202707311,129,000 units
Z-1241-2023BD Ultra-Fine Insulin Syringe 1mL, 6mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326678; GTIN: N/A Lot Number: 2045201, Exp. Date: 20270430; Lot Number: 2073801, Exp. Date: 202705311,168,000 units
Z-1242-2023BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Single Unit Scale-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329461; GTIN: (01) 00382903294619 Lot Number: 2031528, Exp. Date: 20270430686,500 units
Z-1243-2023BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719; GTIN: N/A Lot Number: 2031581, Exp. Date: 203158180,500 units
Z-1244-2023BD Ultra-Fine II Insulin Syringe 0.5mL, 8mm, 30G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326725; GTIN: N/A Lot Number: 2010670, Exp. Date:2031581 Lot Number: 2052365, Exp. Date:202705311,472,400 units
Based on the official FDA remedy

What to do — step by step

  1. Check Syringe Lot Number

    Look for lot numbers 2038580, 2063298, or 2137904 on the syringe packaging.

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 Chile, Colombia, Dominican Republic, Bahamas, Panama, Peru, Mexico, El Salvador, Mexico, Malaysia, Philippines, Vietnam, Hong Kong, Taiwan, Thailand, Canada.” 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 49 days after the firm started it.

1. Firm started the recall: Feb 1, 202312. FDA classified it Class II: Mar 10, 202323. Published in FDA’s Enforcement Report: Mar 22, 202332023
  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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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-1240-2023 (February 1, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1240-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 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