New Medical Technologies recalls 10-pack CryoSolutions cartridges (Model C-CA-23) due to risk of premature valve opening during assembly, potentially emptying the cartridge before use.
During the assembly of the cartridge to its connecting body part, the valve may open prematurely resulting in partial or complete emptying of the cartridge before its intended use.
New Medical Technologies is recalling 10-pack CryoSolutions cartridges (Model C-CA-23) because the valve may open too early during assembly, causing the cartridge to empty before it's supposed to be used. This could lead to the product not working properly when needed.
During cartridge assembly, the valve might open prematurely, causing the cartridge to empty partially or completely before it's intended for use. This could result in the product not functioning as expected when needed for medical procedures.
Users of the CryoSolutions cartridges for medical procedures are affected. Those who have the specific model (C-CA-23) and item number (33516) are most at risk.
Check for the model number C-CA-23 and item number 33516 on the cartridge packaging. The product was sold with specific lot numbers (C6637) and a unique identifier (UDI-DI: 10381780171959).
Verify the model number (C-CA-23) and item number (33516) on the cartridge packaging.
The valve may open prematurely during assembly, causing the cartridge to empty before intended use.
The recall record does not specify a remedy, so check with New Medical Technologies for further instructions.
Look for model number C-CA-23 and item number 33516 on the packaging, or lot number C6637.
We’ve drafted a message you can send New Medical Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1103-2025 — New Medical Technologies New Medical Technologies Hello, I own a New Medical Technologies that is covered by recall Z-1103-2025 from New Medical Technologies. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
