CryoSolutions Cartridges (New Medical Technologies) – Valve Premature Opening (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each), Model: C-CA-23, Item: 33516;
Brand
New Medical Technologies Gmbh Wankdorffeldstrasse
Lot Codes / Batch Numbers
Model: C-CA-23, Item: 33516, UDI-DI: 10381780171959, Lots: C6637.
Products Sold
Model: C-CA-23; Item: 33516; UDI-DI: 10381780171959; Lots: C6637.
New Medical Technologies Gmbh Wankdorffeldstrasse is recalling Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each), Model: C-CA-23, Item: 33516; due to During the assembly of the cartridge to its connecting body part, the valve may open prematurely resulting in partial or complete emptying of the cart. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On December 19, 2024 "Important Notice Regarding Your Device" letters were sent to customers. Corrective Actions: We have implemented the following corrective and preventive actions to address this issue: 1. Enhanced Testing: All cartridges are now being filled with a minimum specified volume (23.5g tolerance) and subjected to rigorous leakage testing. 2. Updated Specifications: We have revised the interface connection specifications to include precise tolerances and correlated these adjustments with the gas volume requirements. 3. Improved Instructions for Use (IFU): Additional safety precautions regarding gas leakage during assembly are now clearly highlighted in the Instructions for Use (IFU) provided with the product. We are committed to ensuring these actions eliminate the identified problem and prevent its recurrence. Our quality assurance team will also verify the effectiveness of these measures by closely monitoring product performance and feedback. What You Should Do: " Please ensure that all users review the updated Instructions for Use (IFU) to familiarize themselves with the additional safety measures, including warnings regarding the potential for premature gas leakage during cartridge connection. Aligned with that the gas cylinder shall be quickly screwed into the handpiece. " Please ensure that a new O-ring is assembled into the body part of the handpiece We sincerely apologize for any inconvenience this may cause and appreciate your understanding and cooperation. If you have any questions or require assistance, please do not hesitate to contact our customer service team. on January 31, 2025, URGENT: VOLUNTARY MEDICAL DEVICE CORRECTION letters were sent out to sub-accounts from their sole consignee. What You Should Do (Customers (i.e. Medical Facility, etc.)): 1. Please review the notice from UMP (Appendix 1). 2. Please ensure that you review the updated Instructions for Use (IFU) to familiarize yourselves with the additional safety measures, incl
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026