Stryker Endoscopy Recalls Fixable Cone for 11mm Hasson Due to Sterilization Labeling
Stryker Endoscopy is recalling 180,573 units of the Fixable Cone for 11mm Hasson because the instructions for use do not support specific sterilization methods.
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: The recall is classified as FDA Class II, and the source text explicitly states no illnesses or injuries are reported, fitting the criteria for a moderate severity score involving labeling or documentation issues.
Plain-English summary
Stryker Endoscopy is recalling 180,573 units of the PKG, FIXABLE CONE FOR 11MM HASSON (P/N 0250080180). These laparoscopic manual instruments are intended for cutting, holding, grasping, and manipulating tissue and organs during surgery. The recall covers units distributed worldwide, including the United States and numerous international locations.
The recall was initiated because the parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods. This is a Class II recall, indicating a situation that could cause temporary or medically reversible health consequences.
Healthcare facilities and distributors should stop using the affected devices and contact Stryker Endoscopy for further instructions. The source text does not report any illnesses or injuries associated with this recall.
The recalled product
- Product
- PKG, FIXABLE CONE FOR 11MM HASSON, P/N 0250080180. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports wh
- Manufacturer
- Stryker Endoscopy
- Affected units
- 180,573
Distribution
Part of a larger recall action
This product is one of 207 recalled by Stryker Endoscopy 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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