Custom Healthcare Systems, Inc. Inpatient Dialysis Kit PAK-19244. Single use. Dialysis kit
FDA Recall Z-0863-2020 · Posted None
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Recalling FirmCustom Healthcare Systems, Inc.
Recall StatusTerminated
Product CodeLRO
Date Initiated2019-12-20
Date Terminated2022-08-01
Product Quantity240 kits
Reason for Recall
A component (1961 TELFA PAD 2 X 3) contains LATEX and was used in the Medical Convenience Kit(PAK-19244). Case label and device label for product did NOT show that the Medical Convenience Kit contained LATEX.
Firm Action
Custom Healthcare Systems, Inc. sent an "Urgent Medical Device Recall" letter dated January 7, 2020 and email message dated January 9, 2020 to its customer. the letter described the product, problem and actions to be taken. Customer was advised to CHECK YOUR INVENTORY AND QUARANTINE ANY AFFECTED PRODUCT. Contact John Chou at 804(421-5959) , or email [email protected], with regards to returning affected products. This recall should be carried out to the end user level. If you have distributed the product further, notify your accounts that received the product of this recall. Remaining product you have available for use should be scheduled for return and replacement or credit compensation. Medical Device Recall Return and Receipt Form provided to consignee for completion and return.
If you have any further questions, contact Quality Assurance Manager, at 804-421-5959 or email: [email protected]
Root Cause
Labeling False and Misleading
Distribution Pattern
US Distribution to IL.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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