Stryker Recalls Expired Arthroscopic Cannulas Due to Labeling Error
Stryker is recalling 10 units of 8.0mm x 90mm Dri-Lok Threaded Cannulas because the expiration date was misprinted as August 2018 instead of August 2016.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall involving a labeling error (incorrect expiration date) with no reported illnesses or injuries, which aligns with the criteria for a Moderate severity score.
Plain-English summary
Stryker Corporation is recalling 10 units of the 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA. The recall involves 2 boxes, with 5 units per box. The product is a disposable cannula designed to be used as a port of entry for arthroscopic instruments into the joints.
The recall was initiated due to an inadvertent shipment of expired units. The expiration date marked on the box is August 2018, but the correct expiration date is August 2016. The affected units are identified by Lot No. 14239AG2 and UPC 07613327055795.
The affected units were distributed in the United States to Massachusetts only. No illnesses or injuries have been reported in connection with this recall.
The recalled product
- Product
- 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.
- Manufacturer
- Stryker Corporation
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 (3)
- Lot No. 14239AG2
- UPC 07613327055795. The expiration date marked on the box is August 2018
- but it should be August 2016.
Distribution
Distributed in 1 state:
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