KeySplint Hard Clear - Indicated for the fabrication of orthodontic and dental appliances such as mouthguards, nightguards, splints, repositioners, and retainers Item No.: 4220011
FDA Recall Z-0630-2024 · Posted 2024-01-03
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Recalling FirmKeystone Industries
Recall StatusOpen, Classified
Product CodeMQC
Date Initiated2023-11-20
Product Quantity336 units
Reason for Recall
Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged with the wrong Instructions for Use. Keysplint Hard Clear were placed inside a zip lock bag along with KeySplint Soft Instructions for Use (IFU).
Firm Action
Keystone Industries issued Urgent Medical Device Recall/Correction letter to Distributors
between 10/20/2023 and 10/23/2023. Letter states reason for recall, health risk and action to take:
For immediate access, the correct IFU is available following this link: 4916111-NATLAB-1372-KeySplint_Hard_DOMESTIC_IFU_WEB.pdf (keystoneindustries.com)
IMMEDIATE ACTIONS TO BE TAKEN
1. Review product inventory and quarantine all affected product on hand. Open
zip lock bag and remove the incorrect IFU. Place an X across the front panel
of the IFU using a marker or pen. Take a picture of the IFU with an X then
discard the IFUs. Record the information on the attached acknowledgement
form.
2. Keystone Industries will send you the correct IFUs for any items remaining in
your inventory upon receipt of the acknowledgement form.
3. Review distribution records and identify all customers who were shipped the
affected product lot.
4. Send End User Notifications provided to you with this notification to all
identified customers that received product. Record evidence of notification on
the acknowledgement form.
Complete the attached Acknowledgement of Medical Device Recall Form and
return within 5 days of receiving this notice. Email the completed form to
[email protected]
If you have any questions after reviewing this notice, please email using the
address below or call Caleb Barylski at 856-548-5205 between 8:00 am and 5:00
pm EST, Monday through Friday.
Root Cause
Labeling mix-ups
Distribution Pattern
Worldwide distribution - US Nationwide and the country of China.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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