Lower riskMedical device recall · FDA · Published October 13, 2022
BD Phoenix PMIC/ID-107 Recall: False antibiotic resistance reports due to minocycline
Becton Dickinson recalls BD Phoenix PMIC/ID-107 panels that may cause false resistance reports in antibiotic tests, delaying treatment. Affected units have specific lot numbers and expiration dates.
Misformulated minocycline-can cause erroneously increased Minimal Inhibitory Concentration (MIC) values when performing antibiotic susceptibility testing (AST) against minocycline and result in the reporting of false resistance for clinical samples if the initial Quality Control (QC) testing of the panel batch passes, delaying treatment of the patient with the most appropriate antibiotic
“BD Phoenix PMIC/ID-107 Recall: False antibiotic resistance reports due to minocycline.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59918-bd-phoenix-pmic-id-107-recall-false-antibiotic-resistance-reports. Based on FDA recall #Z-0232-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0232-2023%22&limit=1).
The FDA announced on Oct. 13, 2022, that Becton Dickinson & Co. is voluntarily recalling BD Phoenix PMIC/ID-107 panels due to misformulation risks. The hazard involves erroneously increased Minimal Inhibitory Concentration values for minocycline testing. Owners should contact the company for further instructions.
How to tell if you have it
BD Phoenix PMIC/ID-107
UPC: 30382904486076
Catalog Number: 448607
Lot Number: 1355046
Expiration Date: 31JAN2023
The hazard
The misformulated minocycline can cause erroneously increased Minimal Inhibitory Concentration values when performing antibiotic susceptibility testing against minocycline. This may result in the reporting of false resistance for clinical samples if initial Quality Control testing passes, potentially delaying appropriate patient treatment.
Context
GovInfoNow's records show Becton Dickinson & Co. has 43 other recalls on record since June 1, 2017. Recent brand recalls include the BD GasP: CO2 Pouch System recall on April 7, 2026, and the BD Kiestra Isolate Suspension Cuvette Array recall on Oct. 23, 2025. Other recent recalls of similar products include the Biomerieux VITEK 2 AST-N447 Kit Recall (June 4, 2026), the HardyDisk AST Cefiderocol 30μg FDC30 recall (June 8, 2026), and the Biomerieux VITEK 2 AST-N461 Test Kit Recall (July 24, 2026).
How to tell if you have this one
Check for the lot number 1355046 and expiration date 31JAN2023 on the panel. The product is sold under catalog number 448607 with specific UDI codes.
Brand
Becton Dickinson
Product
BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Panel Details
Look for lot number 1355046 and expiration date 31JAN2023 on the panel.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
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 41 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-0232-2023 (October 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0232-2023 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.