Stryker recalls T2 Alpha Delta Strike Plate instruments due to potential breakage during nail procedures, which may cause complications. Affected units include specific model and lot numbers.
Instrument can break at the level of the thread when being exposed to high forces during nail implantation or removal which can lead to complications during nail insertion and removal.
Stryker is recalling T2 Alpha Delta Strike Plate instruments used in nail procedures because they can break under high force during implantation or removal, potentially causing complications. This recall affects specific model numbers and lots sold to medical professionals.
The instrument can break at the thread level when exposed to high forces during nail insertion or removal. This breakage may lead to complications during these procedures, such as improper nail placement or tissue damage.
Medical professionals using the Stryker T2 Alpha Delta Strike Plate for nail procedures are most at risk. The recall applies to specific model numbers and lots sold through the manufacturer.
Check for the model number 2351-0050 on the instrument. The recall covers all lots of this product sold with the UDI (Unique Device Identifier) (01)07613327350210.
Inspect the instrument for signs of breakage at the thread level, especially after high-force use during nail procedures.
Reach out to Stryker directly for specific guidance on whether your instrument is affected and how to proceed.
No, this recall is for medical professionals using the instrument in nail procedures.
Check for the model number 2351-0050 and the UDI (01)07613327350210 on the instrument.
Contact Stryker directly for guidance on handling broken instruments.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0780-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0780-2020 from Stryker. 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.
