Reported Nov 23, 2022 · Ongoing
BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most…
Becton Dickinson & Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212
Is this the product you have?
- BD Phoenix PMIC/ID-107The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most aerobic and facultative anaerobic gram-positive bacteria of human origin with selected antimicrobial agents when used with the BD Phoenix Automated Microbiology System
- Catalog (Ref) Number448607
- Lot codes and dates
- UDI(10) 1355046 (17) 230131 (30) 0025 (01) 30382904486076
- Lot Number1355046 Exp
- Date31JAN2023
- Amount recalled
- 13,900 EA
Where it was sold
- Nationwide
Why it was recalled
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
This product could cause temporary or reversible health problems — stop using it.
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