The Recall Desk
ModerateFDA (Devices)·Z-0636-2015·Announced 2014-12-24

Stryker Maryland Forceps Recalled Due to Sterilization Instructions

Stryker Endoscopy is recalling Maryland Forceps 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 hazard is a documentation issue regarding sterilization instructions rather than a direct physical defect or reported injury, fitting the Moderate severity criteria for minor labeling/documentation errors.

Plain-English summary

Stryker Endoscopy is recalling 180,573 units of Maryland Forceps, Curved (P/N 0250080248). These laparoscopic manual instruments are intended for cutting, holding, grasping, and manipulating tissue and organs during surgery. The devices are distributed worldwide, including in the United States and numerous international markets.

The recall was initiated because the parameters provided in the 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 documentation issue affects the ability to properly sterilize the instruments using these specific methods.

Healthcare facilities and distributors should stop using the affected instruments and contact Stryker Endoscopy for further instructions regarding the recall.

The recalled product

Product
PKG, MARYLAND FORCEPS, CURVED, P/N 0250080248. 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 which
Manufacturer
Stryker Endoscopy
Affected units
180,573

Distribution

Distributed nationwide across the United States.

The notice also names 2 states specifically:

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.

See all 207 products in this recall →