Stryker Oasys Midline Occiput Plate-1) Small 2) Medium recall
Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the…
Why was Stryker Oasys Midline Occiput Plate-1) Small 2) Medium recalled?
Stryker has received reports from customers indicating post-operative fracture of the pin that connects the tulip head to the plate body.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
K093670 Catalog numbers: Small - 48551044 Medium - 48551045 Large - 48551046 Large Long - 48551047 Mini- 48551048 All lots of the above
- Product
- Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the…
- Recalling firm
- Stryker Spine
- Quantity
- 1536 units (US) 880 (Foreign)
- Distribution
- Nationwide Distribution.
- Recall date
- August 28, 2013
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)