ABDOMINAL BINDER, 9IN, 3-PANEL, 30-45IN, S/M
Received Mar 12, 2024 · Event occurred Feb 23, 2024
Report 3010452421-2024-00002 · MDR key 18886344
Device
Generic name
Binder, Abdominal
Manufacturer
Ortho & Surgical Products Enterprises S.a.Model number
13661056Product problems
- Patient Device Interaction Problem
- Patient Device Interaction Problem
Patient
NA · Unknown
- Rash
- Rash
Narrative
Additional Manufacturer Narrative
A COMPLAINT WAS RECEIVED ON (B)(6) 2024 REPORTING CUSTOMER STATES SHE HAS HIVES UNDERNEATH UNDER BREAST AND ON BACK. CUSTOMER TAKING BENADRYL FOR REACTION. A SAMPLE IS NOT AVAILABLE TO BE RETURNED TO DEROYAL FOR EVALUATION. A SUPPLIER CORRECTIVE ACTION REQUEST (SCAR) WAS ISSUED TO THE RAW MATERIAL SUPPLIER (B)(4). THIS INVESTIGATION IS ONGOING AT THIS TIME. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. WE WILL PROVIDE FOLLOW-UP REPORT IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Description of Event or Problem
CUSTOMER STATES SHE HAS HIVES UNDERNEATH UNDER BREAST AND ON BACK.
Additional Manufacturer Narrative
A COMPLAINT WAS RECEIVED ON (B)(6) 2024 REPORTING CUSTOMER STATES SHE HAS HIVES UNDERNEATH UNDER BREAST AND ON BACK WHERE BINDER WAS WORN. CUSTOMER TAKING BENADRYL FOR REACTION. A SAMPLE WAS NOT AVAILABLE TO BE RETURNED TO DEROYAL. A SUPPLIER CORRECTIVE ACTION REQUEST (SCAR) WAS ISSUED TO THE RAW MATERIAL SUPPLIER NORTH EAST KNITTING. THE SUPPLIER STATED ALL INTERNAL REQUIRED PROCESS CONTROLS WERE FOLLOWED. THERE HAVE BEEN NO CHANGES MADE TO THE RAW MATERIAL. THE TRUE ROOT CAUSE WAS UNABLE TO BE DETERMINED. DUE TO THE ROOT CAUSE FINDING THERE WERE NO CORRECTIVE AND OR PREVENTIVE ACTIONS TAKEN. THERE HAVE BEEN NO CHANGES MADE TO THE RAW MATERIAL USED FOR THIS ABDOMINAL BINDER. DEROYAL HAS PREVIOUSLY COMPLETED BIOCOMPATIBILITY ON A SIMILAR DEVICE THAT USES THESE MATERIALS THAT WAS ESTABLISHED THAT THESE MATERIALS ARE SAFE TO USE IN CONTACT WITH SKIN. A PERSON MAY HAVE A UNIQUE ALLERGY, BUT THE RISK IS REMOTE. PRODUCT LABELING WAS REVIEWED, AND THE APPROPRIATE SYMBOLS ARE PRESENT CORRECTLY INDICATING THAT THE DEVICE IS NOT MADE WITH NATURAL RUBBER LATEX. PRODUCTION RECORDS WERE REVIEWED, AND NO ISSUES WERE FOUND. A TOTAL OF 50 OF PRODUCT NUMBER 13661056 LOT 60424243 OF THE ABDOMINAL BINDERS WERE RANDOMLY INSPECTED BY DEROYAL, AND NO DISCREPANCIES WERE IDENTIFIED DURING THE INSPECTION. THIS INVESTIGATION IS COMPLETE AT THIS TIME. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. WE WILL PROVIDE FOLLOW-UP REPORT IF ADDITIONAL INFORMATION BECOMES AVAILABLE.