The Recall Desk
HighFDA (Devices)·Z-1664-2017·Announced 2017-04-05

Recall of Sterile Arthroscopy Kits Due to Light Glove Splitting

Resource Optimization & Innovation LLC is recalling 162 sterile arthroscopy kits because a light glove component can split, breaking the sterile field.

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 sterile medical device where a defect can break the sterile field, posing a risk of harm (infection) even though no specific injuries are reported in the source text.

Plain-English summary

Resource Optimization & Innovation LLC is recalling 162 sterile arthroscopy kits (Item Number: 800422004, OR0491D - Arthroscopy Pk - Spohn). The recall is due to a defect in a light glove component included in the custom procedure trays.

The light glove can split during application to a light handle. This failure can break the sterile field, which is a critical safety requirement for surgical procedures. The affected kits were distributed in the United States to locations in California and Texas.

The affected lots have expiration dates of June 20, 2018, August 18, 2018, and November 16, 2018. Healthcare facilities and consumers should stop using these kits and contact the manufacturer for further instructions.

The recalled product

Product
Regard, Item Number: 800422004, Sterile, OR0491D - Arthroscopy Pk - Spohn
Affected units
162

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)

  • 034404D Exp Date 2018-06-20
  • 037483D Exp Date 2018-08-18
  • 039644D Exp Date 2018-11-16

Distribution

Distributed in 2 states:

Part of a larger recall action

This product is one of 135 recalled by Resource Optimization & Innovation Llc 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 135 products in this recall →