Becton Dickinson PCEA Kit ASV Yellow Stripe Microbore Recall: Potential Leaks
Becton Dickinson recalls PCEA Kit ASV Yellow Stripe Microbore (Catalog 10800177) due to potential leaks between male luer lock and tubing. Affected units include specific batch numbers.
Lower-risk recall
The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.
Contact the company
What happened, in plain English
Becton Dickinson is recalling PCEA Kit ASV Yellow Stripe Microbore tubing sets because they may leak between the connection point and the tubing. This leak risk could lead to contamination or improper medication delivery during IV therapy. Read more at govinfonow.com/recall/69767-becton-dickinson-pcea-kit-asv-yellow-stripe-microbore-recall-potential.
Source Summary by GovInfoNow · govinfonow.com/recall/69767-becton-dickinson-pcea-kit-asv-yellow-stripe-microbore-recall-potential · Updated August 20, 2026 · FDA enforcement record: FDA #Z-0387-2019
Cite this page
“Becton Dickinson PCEA Kit ASV Yellow Stripe Microbore Recall: Potential Leaks.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69767-becton-dickinson-pcea-kit-asv-yellow-stripe-microbore-recall-potential. Based on FDA recall #Z-0387-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0387-2019%22&limit=1).
Why it’s dangerous
The tubing may leak between the male luer lock connection and the yellow-striped tubing. This leak could cause medication to escape from the system, potentially leading to contamination or incorrect dosing during IV therapy.
Who’s affected
Healthcare professionals using the PCEA kit for intravenous therapy are most at risk. Patients receiving treatment with this specific tubing set may be affected if leaks occur.
How to tell if you have this one
Check for the yellow striped tubing with anti-siphon valve. The product uses catalog number 10800177 and includes specific batch numbers: 16127933, 17017602, 17055977, 17117153, 17125385, 18015788.
- Brand
Becton Dickinson- Category
Medical device
All 2 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
Terminated- Distribution
Worldwide Distribution - US Nationwide in the states of: AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MO, MT, NC, NE, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and Guam. The products were distributed to the following foreign countries: Canada, United Arab Emirates and Saudi Arabia.
| Recall number | Product, codes & lots |
|---|---|
| Z-0386-2019 | PCEA ASV Yellow Microbore, Catalog Numbers 30893, 30893-07 Product Usage: PCEA Administration Set. Microbore tubing with Yellow Identification Stripe. Anti-siphon valve. Set cannot be used for gravity infusion 1. Connect PCA syringe to female luer on administration set. 2. Push on syringe plunger to prime set. 3. Refer to PCA module directions for Use for complete loading and operating instructions. Notes: The set should be changed according to the facility protocol or in accordance with currently recognized guidelines for IV therapy. Antisiphon sets cannot be primed by gravity.; Batch numbers: 15086977 15095397 15095915 15096391 15096849 15096850 15106576 15106951 15115143 15115716 15115717 16017458 16025336 16025977 16036016 16045460 16045487 16055501 16065137 16065138 16065714 16066549 16067125 16067126 16067127 16067128 16077716 16085262 16085367 15026445 15026291 15026195 15026194 15025581 14116628 14115971 14106583 14106255 14105065 16085368 16087180 16095824 16095862 16096932 16096933 16105618 16107358 16107359 16115132 16125018 16126788 16127223 17015091 17016118 17016119 17017235 17025472 17026261 17026967 17036238 17036239 17056659 17057076 17057077 17065203 17065204 17065249 17066157 15016971 15016044 15015678 14125371 14116627 14056317 14045325 14036825 14036236 14035806 14096716 14096388 14095389 14086964 14085752 14085232 14077092 14076307 14075202 14066846 14066080 14035268 14026691 14026388 14025707 14016290 14016373 14015841 13125080 13116634 13115751 13115436 17085229 17085260 17087278 17096726 17096817 17096818 17096980 17116510 17117476 17117526 17125486 17125487 17125488 17125559 17126893 17126907 18015151 18015152 18015153 18016346 18026103 18026223 18026224 |
| Z-0387-2019 | PCEA Kit ASV Yellow Stripe Microbore, Catalog Number 10800177 Product Usage: PCEA Administration Set. Microbore tubing with Yellow Identification Stripe. Anti-siphon valve. Set cannot be used for gravity infusion 1. Connect PCA syringe to female luer on administration set. 2. Push on syringe plunger to prime set. 3. Refer to PCA module directions for Use for complete loading and operating instructions. Notes: The set should be changed according to the facility protocol or in accordance with currently recognized guidelines for IV therapy. Antisiphon sets cannot be primed by gravity.; Batch numbers: 16127933 17017602 17055977 17117153 17125385 18015788 |
What to do — step by step
Check Product Details
Verify the catalog number 10800177 and batch numbers listed in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 37 states.
FDA distribution: “Worldwide Distribution - US Nationwide in the states of: AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MO, MT, NC, NE, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and Guam. The products were…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Michigan, Missouri, Montana, Nebraska, Nevada, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-0387-2019 (September 26, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0387-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 20, 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.