FDA Adverse Event Other Summary report: N

PALL PXL8 LEUKOCYTE REDUCTION FILTER FOR PLATELETS TRANSFUSI

MDR report key: 116185 · Received August 29, 1997

Report

Report Number
2432733-1997-00038
Event Type
Other
Date Received
August 29, 1997
Date of Event
December 1, 1995
Report Date
July 27, 1997
Manufacturer
PALL BIOMEDICAL PRODUCTS CO.
Product Code
CAK
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE SYMPTOMS OF THE REACTION DESCRIBED COINCIDE WITH MANY OF THOSE KNOWN TO BE ASSOCIATED WITH ANAPHYLACTOID OR IMMEDIATE GENERALIZED REACTION. IMMEDIATE GENERALIZED REACTIONS HAVE BEEN ASSOCIATED WITH PT SENSITIVITY TO THE PLASMA CONSTITUENTS WHICH ACCOMPANY THE PLATELETS DURING INFUSION, IN SUCH PLATELET PREPARATIONS AS CONTAIN PLASMA. IT HAS BEEN REPORTED BY BUCK, ET AL THAT WASHING OF PLATELETS WOULD PREVENT SOME ALLERGIC, BUT NOT FEBRILE, REACTIONS. A REVIEW OF THE LOT MFG HISTORY OR FIELD HISTORY WAS NOT POSSIBLE AS THE DEVICE WAS NEITHER RETAINED NOR IT'S LOT NUMBER RECORDED. IT IS CONCLUDED THAT THE EPISODE REPORTED WAS MOST LIKELY RELATED TO MEDICATIONS EMPLOYED AND/OR THE NATURE OF THE BLOOD PRODUCTS BEING TRANSFUSED TO THIS PT, OR TO UNIDENTIFIED PREDISPOSING FACTORS IN THE PTS IN CONJUNCTION WITH ANY OF THE PRECEDING.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PEDIATRIC PT EXPERIENCED SEVERE HYPOTENSION DURING A TRANSFUSION OF PLATELETS, WHICH WERE FILTERED IN THE BLOOD BANK THROUGH THE DEVICE. THE PT WAS BEING TRANSFUSED AFTER A BONE MARROW TRANSPLANT AND LL LOBOTOMY. THE REPORTER COULD NOT IDENTIFY WHICH OF SEVERAL VARIABLES MIGHT HAVE CAUSED THE HYPOTENSION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PALL PXL8 LEUKOCYTE REDUCTION FILTER FOR PLATELETS TRANSFUSI LEUKOCYTE REDUCTION FILTER FOR PLATELETS CAK PALL BIOMEDICAL PRODUCTS CO. PXL8 UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Required Intervention