The Recall Desk
HighFDA (Devices)·Z-0261-2015·Announced 2014-12-10

Customed Recalls Surgical Gowns Due to Compromised Sterility

Customed, Inc. is recalling 2,520 surgical gowns because compromised sterility and inadequate storage conditions may increase the risk of patient infection.

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 risk-of-harm product (medical device) where the hazard is patient infection due to compromised sterility, but the source text does not report any specific injuries or illnesses, fitting the criteria for a High severity score.

Plain-English summary

Customed, Inc. is recalling 2,520 units of Gown Surgical Non Reinforced XXL (Catalog number 900-2566). These gowns are used by medical staff to perform patient care procedures such as wound healing, suture removals, and wound irrigation. The affected units are identified by Lot number 113036399.

The recall was initiated because the products have compromised sterility, which is not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled, inadequate storage conditions increase the risk of contamination. This contamination may result in patient infection.

The affected products were distributed in the United States to Florida, New York, and Puerto Rico. Medical facilities and consumers should stop using the affected gowns and contact the recalling firm for further instructions.

The recalled product

Product
Gown Surgical Non Reinforced XXL, Catalog number 900-2566. Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.
Manufacturer
Customed, Inc
Affected units
2,520

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)

  • Lot numbers: 113036399

Distribution

Distributed in 3 states:

Part of a larger recall action

This product is one of 179 recalled by Customed, Inc 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 179 products in this recall →