Device recall: regard GS0098C - RESUSABLE RT BRONCH, Item Number: 830086003

FDA enforcement event 90199 · Class II · initiated 3 May 2022 · status Terminated · terminated 27 Jun 2022

DeviceVoluntary: Firm initiated1 product recordRepublic, MO

FDA enforcement event 90199 is a device recall by ROi CPS LLC of Republic, MO, initiated 3 May 2022 and classified Class II, with 1 product record.

FDA defines Class II as 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. 88% of the 839 device enforcement events initiated in 2022 carry the same class.

Status: Terminated, terminated 27 Jun 2022. Initiation: voluntary: firm initiated. ROi CPS LLC has 28 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

ROi CPS LLC, Republic, MO.

Reason for recall

"Convenience kit contained Medline Endoscopy Bedside Cleaning products which were recalled."

Distribution

"FL"

Product records

Recall number	Product	Quantity	Class	Status	Report date
Z-1255-2022	regard GS0098C - RESUSABLE RT BRONCH, Item Number: 830086003	24 kits	Class II	Terminated	15 Jun 2022

Context

88%of 2022 device events are Class II839 events that year

1product record in this eventfirm median: 1

28events on this register for the firm

Other enforcement events for ROi CPS LLC

Initiated	Product (first record)	Type	Class	Records
26 Dec 2024	regard Item Number: 830106006, LD01114F - Newborn Kit containing the component Neo-Tee Resuscitator. Convenience kit to	Device	Class I	1
24 Jul 2024	regard Clinical Packaging Solutions, HT00376I - SPECIAL PROCEDURE, Item Number 800223009	Device	Class II	1
17 Jun 2024	Regard Kit containing the Microtek decanter	Device	Class II	1
18 Dec 2023	regard Operative LAP, Item Number 800943001; surgical convenience kit	Device	Class I	1
20 Nov 2023	Regard Dressing change kit, Item Number 800026006	Device	Class I	1
21 Sep 2023	Regard CV PK, Item Numbers a) 880289014, b) 880289015; cardiovascular convenience kit	Device	Class II	1
11 Sep 2023	GS0008 2Y - Burn Pack - STL, Item Number 880082025	Device	Class II	1
22 Mar 2023	Sterile surgical convenience kits: 1. regard Item Number: 880405003, GS01011C - General Laparoscopy; 2. regard Item Numb	Device	Class II	8
20 Oct 2022	regard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kit	Device	Class II	40
3 Jun 2022	Nonsterile convenience kits: (1) regard Item #830099008, CV01005H - CV Part 1 Bundle; and (2) regard Item #830019017, CV	Device	Class II	2

All 28 events for ROi CPS LLC

Questions and answers

Why was this device recalled?

FDA's record gives the reason for recall as: "Convenience kit contained Medline Endoscopy Bedside Cleaning products which were recalled."

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. 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.

Where was the product distributed?

FDA's distribution pattern field reads: "FL"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 27 Jun 2022. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.