The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-2637-2015·Announced 2015-09-09

Customed Urology Surgical Packs Recalled for Sterilization Validation Issues

Customed, Inc. is recalling 450 Urology Surgical Packs distributed in Puerto Rico due to inadequate validation of sterilization processes and package integrity.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

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 (sterile surgical packs) where the hazard is theoretical (inadequate sterilization validation) and no injuries or illnesses have been reported, fitting the 'High' severity criteria.

Plain-English summary

Customed, Inc. is recalling 450 units of Urology Surgical Packs (Code 9002510) that were distributed exclusively in Puerto Rico. The recall was initiated because of inadequate validation and qualification of the sterilization processes and package integrity for products released for distribution as sterile.

The affected lots include 141015726, 141216304, 150116542, 150317833, 150317834, 150317835, 150317836, 150317837, 150317838, 150418370, and 150418371. These products are used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, and wound irrigation.

The source text does not specify any reported illnesses or injuries associated with these products. Medical facilities and consumers in Puerto Rico should stop using these specific lots and contact the recalling firm or the FDA for further instructions.

The recalled product

Product
UROLOGY SURGICAL PACK 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Manufacturer
Customed, Inc
Affected units
450

Distribution

Distributed in 1 state:

Part of a larger recall action

This product is one of 170 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 170 products in this recall →

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