Lower riskMedical device recall · FDA · Published May 19, 2020
ROi CPS Respirator Crash Cart Kit: Incorrect Expiration Date Labeling
ROi CPS recalls specific Respirator Crash Cart Kits with incorrect expiration dates that may expire before other components. Affected kits have lot numbers 77127, 74813, and 63168. Contact for replacement.
Roi CPS, LLC has become aware of a labeling error that affects select custom procedure kits. The kits are labeled with an expiration date that is later than that of the soonest kit component to expire in the kits.
Take action
Contact the company
📍Recalling firmROi CPS LLC3000 E Sawyer Rd · Republic, MO 65738-2758
“ROi CPS Respirator Crash Cart Kit: Incorrect Expiration Date Labeling.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65120-roi-cps-respirator-crash-cart-kit-incorrect-expiration-date-labeling. Based on FDA recall #Z-2466-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2466-2020%22&limit=1).
ROi CPS LLC voluntarily recalled the Respirator Crash Cart Kit on May 19, 2020, after the FDA announced a labeling error regarding expiration dates. The kits were distributed exclusively in Missouri and Louisiana.
How to tell if you have it
Brand: ROi CPS
Product: Respirator Crash Cart Kit
Item #: 830066
Lot #: 77127, 74813 and 63168
The hazard
The kits are labeled with an expiration date that is later than that of the soonest kit component to expire in the kits. The FDA said this labeling error affects select custom procedure kits.
Context
GovInfoNow's records show ROi CPS LLC has 27 other recalls on record since Jan. 3, 2020. Other recent recalls of similar products include ROi CPS Newborn Kit Recall (Dec. 26, 2024), ROi CPS Recalls Medical Convenience Kits with Merit Syringes - Safety Risk (July 24, 2024) and ROi CPS Regard Kit Microtek Decanter Recall: Pin Holes in Sterile Packaging (June 17, 2024). Other recent recalls of similar products include B Braun Discofix Four Way Stopcock Recall (Aug. 4, 2026), Urinary Clean Catch Kit Recalled Due to Incorrect Expiration Date (July 9, 2026) and Inspire Respiratory Sensing Lead Model 4340: Incorrect Use By Date May Cause Unplanned Surgery (May 11, 2026).
How to tell if you have this one
Check the lot number on the kit: 77127, 74813, or 63168. The expiration date on the kit label should match the specific date listed for each lot.
Brand
ROi CPS
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
Domestic distribution only to: MO and LA.
Recall number
Product, codes & lots
Quantity
Z-2465-2020
Isolation Droplet Bundle Kit; Item: 830006013, Lot #: 78253M
24 kits
Z-2466-2020
Respirator Crash Cart Kit; Item #: 830066; Lot #: 77127, 74813 and 63168 Expiration date per lot: Lot: 77127, Exp date: 1/31/2021 Lot: 74813, Exp date: 8/30/2021 Lot: 63168, Exp date: 1/30/2021
200 kits
Based on the official FDA remedy
What to do — step by step
Check Kit Lot Number
Look for lot numbers 77127, 74813, or 63168 on the kit label.
Where it went and when
Where it was distributed
Distributed in Louisiana and Missouri.
Listed by the agency
Not listed
FDA distribution: “Domestic distribution only to: MO and LA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Louisiana, Missouri.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2466-2020 (May 19, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2466-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.