SEASPINE ORTHOPEDICS CORPORATION recalls Daytona Small Stature Ti Lock: Manufacturing defects may prevent proper component mating. Affected model 79-0001 sold with lot numbers MM2098114B.
Due to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
SEASPINE ORTHOPEDICS CORPORATION is recalling Daytona Small Stature Ti Locking Caps 4.5mm (model 79-0001) due to manufacturing defects that could prevent proper component mating. This issue may lead to improper function of the product.
The locking caps have manufacturing defects that can cause components to not mate properly. This may lead to improper function of the product, but does not indicate immediate danger to users.
People who own or use Daytona Small Stature Ti Locking Caps 4.5mm (model 79-0001) with lot numbers MM2098114B are affected. Those using these components in medical applications may be at slightly higher risk due to potential improper function.
Check for the model number 79-0001 on the product. Lot numbers MM2098114B are associated with this recall.
Verify the model number and lot number to confirm if your product is affected.
The recall states there is a manufacturing defect that may affect component mating, but it does not indicate immediate safety risks. Users should check if their product is affected.
The recall does not specify a remedy, so check the product details to see if it is affected. If affected, contact the manufacturer for further instructions.
Look for model number 79-0001 and lot number MM2098114B on the product.
We’ve drafted a message you can send Daytona Small Stature to request your refund or repair — edit it as you like.
Subject: Recall Z-0752-2025 — Daytona Small Stature Daytona Small Stature Hello, I own a Daytona Small Stature that is covered by recall Z-0752-2025 from Daytona Small Stature. 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.
