A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For fracture fixation or reconstruction of the sternum.
FDA Recall Z-0242-2020 · Posted None
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Recalling FirmAlto Development Corp
Recall StatusTerminated
Product CodeJDQ
Date Initiated2019-09-10
Date Terminated2020-05-12
Product Quantity209 total
Reason for Recall
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner inoperable.
Firm Action
On September 10, 2019, the firm distributed a letter to customers titled Product Recall: Action Required.
The letter informed customers of the potential tensioner failure. Customers were given two options:
1. A&E will provide a supply of individually packaged, sterile tensioners to be kept on hand should a kit tensioner be found inoperable. Surgeons and Operating Room staff need to be alerted to this situation and the stock of additional tensioners readily available to them during surgery.
2. For those customers who prefer to return their affected lots of Thorecon, A&E will provide a Returned Goods Authorization and replacement product (to be provided as soon as inventory is available).
Any failed tensioners can be discarded.
Customers were asked to complete and return the acknowledgement form included with the mailing.
Should you have any questions about the action or the product, please contact your A&E Sales Representative or our Customer Service at 800-323-4035.
Root Cause
Process control
Distribution Pattern
Distributed to AL, CA, FL, GA, IL, LA, MO, OK, MS, NM, OK, SC, TX, UT, VT, WA, and WI.
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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