Recall StatusTerminated
Date Initiated2018-06-21
Date Terminated2019-07-09
Product Quantity10,360 plates
Reason for Recall
A portion of this lot was manufactured using Gentamicin instead of Vancomycin. Gentamicin is an inhibitory agent of Neisseria organisms. This
product is a selective plated medium to provide enhanced growth and recovery of N
gonorrhoeae. Inhibited growth may cause a false negative result or a delayed result leading to
incorrect or delayed treatment.
Firm Action
The firm, BD Diagnostic System, sent an "URGENT MEDICAL DEVICE PRODUCT RECALL" letter dated June 21, 2018, to its customers via UPS, to the attention of Microbiology Manager/Supervisor. The letter described the product, problem and actions to be taken. The customers were instructed to do the following:
I. Complete the Customer Response Form and return to the BD contact noted on the form whether or not you have any of the impacted material so that BD may acknowledge your receipt of this notification.
2. Discard any remaining inventory of lot 8110781 . BD will process replacement of any discarded inventory upon receipt of the Customer Response Form.
3. Share this Recall Letter with all users of the product within your facility to ensure awareness.
BD has identified the root cause of this situation and has initiated corrective actions to prevent
recurrence in the future.
If you require further assistance, please contact: 800-638-8663
Customer/Technical Support Monday- Friday between 7:00am and 7:00pm (EST) in the United States.
Root Cause
Under Investigation by firm
Distribution Pattern
US Distribution in states of: AK, AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, ID, IN, KS, KY, MA, MI, MS, MT, NC, JH, NY, OK, OR, PA, SC, TN, TX, WA, and WI.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.