Resource Optimization & Innovation Recalls Sterile Head and Neck Surgical Kits
Resource Optimization & Innovation LLC is recalling 381 sterile Head & Neck surgical kits because the equipment glove component may contain splits or holes that compromise sterility.
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 kits) where the hazard is 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
Resource Optimization & Innovation LLC is recalling 381 sterile Head & Neck surgical kits (Item Number 800559, ET0648). The kits contain surgical instruments and accessories intended for use during surgical procedures. The recall was initiated because the kits contain an equipment glove component which may contain splits or holes, potentially compromising the sterility of the product.
The affected lots are 17581, 19365, 20418, 22472, 23381, and 24400. Distribution was made to Louisiana, Mississippi, and Texas. The responsible firm on the label is ROi, LLC, located in St. Louis, MO.
Healthcare facilities and consumers should stop using these kits immediately and contact Resource Optimization & Innovation LLC for instructions on return or replacement.
The recalled product
- Product
- regard Item Number: 800559, Sterile, ET0648 - Head & Neck - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical…
- Manufacturer
- Resource Optimization & Innovation Llc
- Category
- Medical Device — Surgical Kits
- Affected units
- 381
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 (6)
- Lot numbers 17581
- 19365
- 20418
- 22472
- 23381
- and 24400.
Distribution
Part of a larger recall action
This product is one of 77 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.
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