Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture
Ossur H / F is recalling Lil Angel Vest P2 Lambswool units because the plastic stabilizer strap may partially or completely fracture.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device with a structural defect (fracture of a stabilizer strap) that poses a risk of harm to patients, but the source text does not report any specific injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.
Plain-English summary
Ossur H / F is recalling the Ossur Lil Angel Vest P2 Lambswool. This pediatric-sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
The recall is being issued because there is a potential for partial or complete fracture of the plastic stabilizer strap on the vest. The affected units are identified by part number 545100L and were manufactured from 2008 to the current date.
A total of 435 units across all models are included in this recall. The products were distributed nationwide in the United States and in Hong Kong. Consumers should stop using the affected vests and contact the recalling firm for instructions on how to proceed.
The recalled product
- Product
- Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
- Manufacturer
- Ossur H / F
- Affected units
- 435
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- P/N: 545100L units from 2008 to current
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 6 recalled by Ossur H / F under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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