Custom procedure kits recalled over inflation handles that may detach
Merit Medical Systems is recalling its Custom Procedure Kit because the inflation device handle may detach from the syringe during a procedure.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Scored 3 under the risk-of-harm criterion: the firm states the inflation device handle may detach during a procedure, and no injuries are reported.
Plain-English summary
The Merit Medical Custom Procedure Kit is being recalled by Merit Medical Systems, Inc., covering reference numbers K12T-04270A, K12T-07956 and K12T-10922B.
The reason given in the enforcement record is that the inflation device handle may detach from the syringe during a procedure.
The record does not state a quantity. UDI and lot numbers are recorded in the enforcement record. Distribution was worldwide, including nationwide in the United States across a wide range of states. The FDA has classified the action as Class II.
A device component that detaches mid-procedure can interrupt the procedure. The enforcement record reports no injuries. Facilities should quarantine affected kits and follow Merit Medical's instructions.
The recalled product
- Product
- Merit Medical , Custom Procedure Kit Reference Numbers: K12T-04270A K12T-07956 K12T-10922B
- Manufacturer
- Merit Medical Systems, Inc.
- Category
- Medical Device — Procedure kit
Distribution
Part of a larger recall action
This product is one of 7 recalled by Merit Medical Systems, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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