Lower riskMedical device recall · FDA · Published April 30, 2021
RanD Hang&Go Kit Recall: Possible Non-Sterile Products
RanD recalls Hang&Go kits (Reference Code R9900120) with specific lot numbers due to possible non-sterile products. Affected users should check their lot numbers and contact RanD for guidance.
The sterilization contractor informed the company of a quality issue possibly affecting the sterilization process of a certain number of products. It was determined that some lots may not be sterile.
“RanD Hang&Go Kit Recall: Possible Non-Sterile Products.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62630-rand-hang-go-kit-recall-possible-non-sterile-products. Based on FDA recall #Z-2048-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2048-2021%22&limit=1).
RanD S.r.l. recalled Hang&Go kits for hyperthermic perfusion due to potential non-sterility, the FDA said on April 30, 2021. The agency announced the Class II voluntary recall after a sterilization contractor identified a quality issue affecting specific lots.
How to tell if you have it
Brand: RanD
Product: Hang&Go (kit for hyperthermic perfusion)
Reference Code: R9900120
Lot Numbers: F180266, F180315, F190169
Quantity: 72 units
Distribution: FL, IL, TN, WI
The hazard
The sterilization contractor informed the company of a quality issue possibly affecting the sterilization process. It was determined that some lots may not be sterile.
Context
GovInfoNow's records show other recent recalls of similar products include Medline Convenience Kits Recall: Risk of Contaminated Sterile Products (2026-01-07), Medline Convenience Kits Recall: Sterility Risk from Calibration Issues (2026-01-07), and Medline Convenience Kits Recall: Risk of Sterile Packaging Breach (2026-06-12).
How to tell if you have this one
Check the lot numbers on your Hang&Go kit: F180266, F180315, or F190169. The kits were sold with Reference Code R9900120.
Brand
RanD
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
The products were distributed to the following US states: FL, IL, TN, WI
Recall number
Product, codes & lots
Quantity
Z-2048-2021
Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120; Lot Numbers: F180266 F180315 F190169
72
Z-2049-2021
Ch24 round silicone catheter, Diameter: 8 mm, Perforated section: 230 mm, Total length: 600 mm, Reference Code R9900099. Thoracic/abdominal cavity drain catheter.; Lot Numbers: F180264
40
Based on the official FDA remedy
What to do — step by step
Check Lot Numbers
Identify your kit's lot number from the list: F180266, F180315, or F190169.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “The products were distributed to the following US states: FL, IL, TN, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Illinois, Tennessee, Wisconsin.
Recall timeline
FDA terminated this recall 2.8 years 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-2048-2021 (April 30, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2048-2021 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.