BD Phoenix Panel NMIC-312 Recall: Risk of Klebsiella Pneumoniae Contamination
Becton Dickinson recalls 553,625 BD Phoenix Panel NMIC-312 units due to potential Klebsiella pneumoniae ATCC BAA-1705 contamination in CPO Ambler classification feature.
Recall notice
Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.
What happened, in plain English
Becton Dickinson is recalling 553,625 units of the BD Phoenix Panel NMIC-312 laboratory device because it may contain Klebsiella pneumoniae ATCC BAA-1705 bacteria when used with the CPO Ambler classification feature. This could lead to infections if the bacteria are introduced into patient samples. Read more at govinfonow.com/recall/1764899-becton-dickinson-co-recalls-bd-phoenix-panel-nmic-312-catalog.
Source Summary by GovInfoNow · govinfonow.com/recall/1764899-becton-dickinson-co-recalls-bd-phoenix-panel-nmic-312-catalog · Published October 27, 2026 · Updated October 27, 2026 · FDA enforcement record: FDA #Z-0139-2027
Cite this page
“BD Phoenix Panel NMIC-312 Recall: Risk of Klebsiella Pneumoniae Contamination.” GovInfoNow, updated October 27, 2026. https://govinfonow.com/recall/1764899-becton-dickinson-co-recalls-bd-phoenix-panel-nmic-312-catalog. Based on FDA recall #Z-0139-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0139-2027%22&limit=1).
Why it’s dangerous
The device may fail quality control during the CPO Ambler classification process, potentially introducing Klebsiella pneumoniae ATCC BAA-1705 bacteria into patient samples. This could lead to infections if the bacteria are not properly controlled during testing.
Who’s affected
Users of the BD Phoenix Panel NMIC-312 laboratory device who perform CPO Ambler classification tests are affected. Healthcare facilities using this product for laboratory testing are most at risk.
How to tell if you have this one
Check for the catalog number 449082 or UDI numbers listed in the recall notice. The affected units have specific lot numbers including 5324466, 5349874, and others.
- 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
Ongoing- Distribution
US Nationwide distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0139-2027 | BD Phoenix Panel NMIC-312. Catalog Number: 449082.; Catalog Number: 449082. UDI Numbers: (10)5324466(17)26 1116(30)0025(01)3 0382904490820, (10)5349874(17)26 1209(30)0025(01)3 0382904490820, (10)6008828(17)26 1226(30)0025(01)3 0382904490820, (10)5350977(17)26 1228(30)0025(01)3 0382904490820, (10)6028392(17)27 0120(30)0025(01)3 0382904490820, (10)6034513(17)27 0131(30)0025(01)3 0382904490820, (10)6042998(17)27 0202(30)0025(01)3 0382904490820, (10)6042021(17)27 0203(30)0025(01)3 0382904490820, (10)6056431(17)27 0217(30)0025(01)3 0382904490820, (10)6069033(17)27 0309(30)0025(01)3 0382904490820, (10)6083447(17)27 0327(30)0025(01)3 0382904490820, (10)6098295(17)27 0330(30)0025(01)3 0382904490820, (10)6104811(17)27 0412(30)0025(01)3 0382904490820, (10)6104042(17)27 0419(30)0025(01)3 0382904490820, (10)6118556(17)27 0421(30)0025(01)3 0382904490820, (10)6125526(17)27 0501(30)0025(01)3 0382904490820, (10)6128740(17)27 0503(30)0025(01)3 0382904490820, (10)6132650(17)27 0508(30)0025(01)3 0382904490820, (10)6132735(17)27 0510(30)0025(01)3 0382904490820, (10)6148198(17)27 0518(30)0025(01)3 0382904490820, (10)6148397(17)27 0524(30)0025(01)3 0382904490820, (10)6153088(17)27 0525(30)0025(01)3 0382904490820, (10)6153231(17)27 0526(30)0025(01)3 0382904490820, (10)6160397(17)27 0602(30)0025(01)3 0382904490820, (10)6160450(17)27 0605(30)0025(01)3 0382904490820, (10)6166259(17)27 0604(30)0025(01)3 0382904490820, (10)6166265(17)27 0606(30)0025(01)3 0382904490820, (10)6181978(17)27 0622(30)0025(01)3 0382904490820, (10)6181006(17)27 0623(30)0025(01)3 0382904490820, (10)6181015(17)27 0623(30)0025(01)3 0382904490820, (10)6181164(17)27 0626(30)0025(01)3 0382904490820, (10)6181151(17)27 0626(30)0025(01)3 0382904490820, (10)6181991(17)27 0622(30)0025(01)3 0382904490820, (10)6188614(17)27 0703(30)0025(01)3 0382904490820, (10)6188641(17)27 0703(30)0025(01)3 0382904490820, (10)6188683(17)27 0705(30)0025(01)3 0382904490820, (10)6188905(17)27 0710(30)0025(01)3 0382904490820, (10)6188922(17)27 0711(30)0025(01)3 0382904490820, (10)6195847(17)27 0713(30)0025(01)3 0382904490820, (10)6195877(17)27 0714(30)0025(01)3 0382904490820. Lot Numbers: 5324466, 5349874, 6008828, 5350977, 6028392, 6034513, 6042998, 6042021, 6056431, 6069033, 6083447, 6098295, 6104811, 6104042, 6118556, 6125526, 6128740, 6132650, 6132735, 6148198, 6148397, 6153088, 6153231, 6160397, 6160450, 6166259, 6166265, 6181978, 6181006, 6181015, 6181164, 6181151, 6181991, 6188614, 6188641, 6188683, 6188905, 6188922, 6195847, 6195877. | 553,625 units |
| Z-0140-2027 | BD Phoenix Panel NMIC-306. Catalog Number: 449292.; Catalog Number: 449292. UDI Numbers: (10)5301934(17)26 1102(30)0025(01)3 0382904492923, (10)5301046(17)26 1107(30)0025(01)3 0382904492923, (10)5301019(17)26 1105(30)0025(01)3 0382904492923, (10)5301058(17)26 1108(30)0025(01)3 0382904492923, (10)5301088(17)26 1109(30)0025(01)3 0382904492923, (10)5324448(17)26 1111(30)0025(01)3 0382904492923, (10)5325592(17)26 1122(30)0025(01)3 0382904492923, (10)5336528(17)26 1125(30)0025(01)3 0382904492923, (10)5336554(17)26 1130(30)0025(01)3 0382904492923, (10)5336667(17)26 1203(30)0025(01)3 0382904492923, (10)5336716(17)26 1206(30)0025(01)3 0382904492923, (10)5343520(17)26 1209(30)0025(01)3 0382904492923, (10)5343522(17)26 1221(30)0025(01)3 0382904492923, (10)5350942(17)26 1226(30)0025(01)3 0382904492923, (10)5350876(17)26 1223(30)0025(01)3 0382904492923, (10)5350972(17)26 1228(30)0025(01)3 0382904492923, (10)6006439(17)26 1231(30)0025(01)3 0382904492923, (10)6006497(17)27 0104(30)0025(01)3 0382904492923, (10)6006475(17)27 0103(30)0025(01)3 0382904492923, (10)6013345(17)27 0111(30)0025(01)3 0382904492923, (10)6013300(17)27 0109(30)0025(01)3 0382904492923, (10)6013963(17)27 0118(30)0025(01)3 0382904492923, (10)6013924(17)27 0117(30)0025(01)3 0382904492923, (10)6034519(17)27 0131(30)0025(01)3 0382904492923, (10)6042012(17)27 0203(30)0025(01)3 0382904492923, (10)6042040(17)27 0204(30)0025(01)3 0382904492923, (10)6042153(17)27 0208(30)0025(01)3 0382904492923, (10)6069030(17)27 0309(30)0025(01)3 0382904492923, (10)6082661(17)27 0313(30)0025(01)3 0382904492923, (10)6098326(17)27 0331(30)0025(01)3 0382904492923, (10)6098427(17)27 0405(30)0025(01)3 0382904492923, (10)6104765(17)27 0411(30)0025(01)3 0382904492923, (10)6125411(17)27 0427(30)0025(01)3 0382904492923, (10)6128662(17)27 0430(30)0025(01)3 0382904492923, (10)6138197(17)27 0505(30)0025(01)3 0382904492923, (10)6148207(17)27 0519(30)0025(01)3 0382904492923, (10)6148231(17)27 0520(30)0025(01)3 0382904492923. Lot Numbers: 5301934, 5301046, 5301019, 5301058, 5301088, 5324448, 5325592, 5336528, 5336554, 5336667, 5336716, 5343520, 5343522, 5350942, 5350876, 5350972, 6006439, 6006497, 6006475, 6013345, 6013300, 6013963, 6013924, 6034519, 6042012, 6042040, 6042153, 6069030, 6082661, 6098326, 6098427, 6104765, 6125411, 6128662, 6138197, 6148207, 6148231. | 669,200 units |
What to do — step by step
Stop Using Immediately
Discontinue use of the BD Phoenix Panel NMIC-312 if it has the catalog number 449082 or the listed UDI numbers and lot numbers.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
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-0139-2027 (August 13, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0139-2027 to see it in context.
- Plain-language summary written by qwen3:4b on October 27, 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.