MAUDE Adverse Event Report: BECTON, DICKINSON & CO. (SPARKS) BD BBL¿ GROUP A SELECTIVE STREP AGAR W/5% SHEEP BLOOD (SSA¿); CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL

Catalog Number	221780
Medical Device Problem Code	Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/12/2022
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
A device evaluation and/or device history review is anticipated but is not complete.Upon completion, a supplemental report will be filed.
Event or Problem Description
It was reported that before use of bd bbl¿ group a selective strep agar w/5% sheep blood (ssa¿) biological contamination was found.This is a report of 1 occurrence.As the issue was discovered before use there were no results to report.The following information was provided by the initial reporter: contamination is reported with lot #2054985 - 221780.
Event or Problem Description
It was reported that before use of bd bbl¿ group a selective strep agar w/5% sheep blood (ssa¿) biological contamination was found.This is a report of 1 occurrence.As the issue was discovered before use there were no results to report.The following information was provided by the initial reporter: contamination is reported with lot #2054985 - 221780.
Additional Manufacturer Narrative
H.6 investigation summary: during manufacturing of material 221780, media is formulated and sent through a high temperature short time sterilizer to remove bioburden.The petri dishes are subjected to uv radiation to decrease bioburden.The petri dishes are filled in a positive pressure hepa filtered environment.The filled plates are cooled and immediately wrapped into sleeves to decrease the introduction of microbes.Sleeves are then packaged into cartons and then transferred to a refrigerated truck (2 to 8 degrees c) for shipment to the distributor.Bd distributors are provided with the storage guidelines for the shipping and handling of bd media of 2 to 8 degrees c in a dark place.The batch history record review for batch 2054985 was satisfactory and no quality notifications were generated during manufacturing and inspection.The release testing that is performed on this product does include physical attribute and bioburden testing.A sample of plates are incubated at 25 degrees c and at 35 degrees c for approximately 72 hours.All physical attribute and bioburden testing performed on this batch was satisfactory per bd internal procedures.Affected product does not have any sterility claims; the product is.Tested for bioburden prior to release to ensure that it conforms to product specifications.However, this does not ensure that the end-user will not receive a contaminated plate.The complaint history was reviewed, and no other complaints have been taken on batch 2054985.No retention samples for this batch were available for investigation.Two photos were received.Photo 1 shows a plate with larger black growth with white corona; no id visible on side of plate shown.Photo 2 shows id 2054985 timestamp 0231 with growth showing on other side of plate.No return samples were received for investigation of this complaint.This complaint can be confirmed.No complaint trends for this defect have been identified for this product; no actions are indicated at this time.Bd will continue to trend complaints for contamination.

• Brand Name: BD BBL¿ GROUP A SELECTIVE STREP AGAR W/5% SHEEP BLOOD (SSA¿)
• Common Device Name: CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL
• Manufacturer (Section D): BECTON, DICKINSON & CO. (SPARKS); 7 loveton circle; sparks MD 21152
• Manufacturer (Section G): BECTON, DICKINSON & CO. (SPARKS); 7 loveton circle; sparks MD 21152
• Manufacturer Contact: phillip emmert ; 9450 south state street; sandy, UT 84070 ; 8015296192
• MDR Report Key: 14415384
• Report Number: 1119779-2022-00705
• Device Sequence Number: 5499986
• Product Code: JSI
• UDI-Device Identifier: 00382902217800
• UDI-Public: 382902217800
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K840294
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/01/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Expiration Date: 07/05/2022
• Device Catalogue Number: 221780
• Device Lot Number: 2054985
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/12/2022
• Supplement Date Received by Manufacturer: 09/01/2022
• Initial Report FDA Received Date: 05/17/2022
• Supplement Report FDA Received Date: 09/16/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 02/23/2022
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown