Becton Dickinson BD Phoenix Panels NMIC-306 and NMIC-312
BD Phoenix Panel NMIC-312 may have quality control failures with Klebsiella pneumoniae.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Becton Dickinson & Co. recalled BD Phoenix Panel NMIC-312 and BD Phoenix Panel NMIC-306 due to potential quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature. The company began the recall on August 13, 2026, and the FDA added it to the Enforcement Report on October 9, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI, lot code and catalog code are listed under that product.
Incomplete list: 80 of 154 UDI-DIs shown.
BD Phoenix Panel NMIC-312.
- UDI-DI
- 5324466
- 1116
- 0025
- 0382904490820
- 5349874
- 1209
- 6008828
- 1226
- 5350977
- 1228
- 6028392
- 0120
- 6034513
- 0131
- 6042998
- 0202
- 6042021
- 0203
- 6056431
- 0217
- 6069033
- 0309
- 6083447
- 0327
- 6098295
- 0330
- 6104811
- 0412
- 6104042
- 0419
- 6118556
- 0421
- 6125526
- 0501
- 6128740
- 0503
- 6132650
- 0508
- 6132735
- 0510
- Catalog code
- 449082.
- Lot
- 6148198
- 6148397
- 6153088
- 6153231
- 6160397
- 6160450
- 6166259
- 6166265
- 6181978
- 6181006
- 6181015
- 6181164
- 6181151
- 6181991
- 6188614
- 6188641
- 6188683
- 6188905
- 6188922
- 6195847
- 6195877
BD Phoenix Panel NMIC-306.
- UDI-DI
- 5301934
- 1102
- 0025
- 0382904492923
- 5301046
- 1107
- 5301019
- 1105
- 5301058
- 1108
- 5301088
- 1109
- 5324448
- 1111
- 5325592
- 1122
- 5336528
- 1125
- 5336554
- 1130
- 5336667
- 1203
- 5336716
- 1206
- 5343520
- 1209
- 5343522
- 1221
- 5350942
- 1226
- 5350876
- 1223
- 5350972
- 1228
- 6006439
- 1231
- 6006497
- 0104
- 6006475
- 0103
- Catalog code
- 449292.
- Lot
- 6013345
- 6013300
- 6013963
- 6013924
- 6034519
- 6042012
- 6042040
- 6042153
- 6069030
- 6082661
- 6098326
- 6098427
- 6104765
- 6125411
- 6128662
- 6138197
- 6148207
- 6148231
Details
- Company began the recall
- Event ID
- 99725
- Company
- Becton Dickinson & Co.
- Hazard
- Device defect
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
