Lower riskMedical device recall · FDA · Published June 29, 2026
American Contract Systems Convenience Kit Recall: Catheters May Not Meet Performance
American Contract Systems recalls Convenience Kit CV B PACK (Model TNCB10AN) due to catheters not meeting performance specs. Affected units sold until Jan 2027.
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable performance specifications.
“American Contract Systems Convenience Kit Recall: Catheters May Not Meet Performance.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697977-american-contract-systems-convenience-kit-recall-catheters-may-not-meet. Based on FDA recall #Z-3001-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3001-2026%22&limit=1).
The FDA announced on June 29, 2026, that American Contract Systems Inc is recalling the American Contract System Convenience Kit, CV B PACK (Model TNCB10AN) due to catheters failing performance specifications. Owners should contact the company for a remedy.
How to tell if you have it
Brand: American Contract Systems
Product: American Contract System Convenience Kit, CV B PACK
Model/Catalog Number: TNCB10AN
Lot Code: 42-8768511
UDI: 191072239907
Expiration Date: 1/6/2027
The hazard
The kits contain Medline Red Rubber Intermittent Catheters and Trays. Representative samples did not meet applicable performance specifications, according to the FDA.
Context
GovInfoNow's records show American Contract Systems Inc has 21 other recalls on record since November 21, 2018. Other recent recalls of similar products include Medical convenience kits containing BD CliniClean Pericare Wipes (August 10, 2026), Medical Kits with potential endotoxin variability (May 19, 2026), and Convenience Kits with risk of blood exposure (March 19, 2026). Other recent recalls of similar products include Medline Medical Procedure Kits recalled for catheter issues on May 4, 2026.
How to tell if you have this one
Check for the model number TNCB10AN on the kit. The lot code 42-8768511 and expiration date of January 6, 2027 are also on the kit.
Brand
American Contract Systems
Category
Medical device
FDA recall event · 4 products
All 4 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
Ongoing
Distribution
US Nationwide distribution in the states of IA, OH.
Recall number
Product, codes & lots
Quantity
Z-3000-2026
American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM; Lot Code: Lot Number: 42-8493811 UDI: 191072232991 Expiration Date: 7/15/2026
30 units
Z-3001-2026
American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN; Lot Code: Lot Number: 42-8768511 UDI: 191072239907 Expiration Date: 1/6/2027
30 units
Z-3002-2026
American Contract System Convenience Kits, CV B PACK, Model/Catalog Number: TNCB10AP; Lot Code: Lot Number: 42-8808611 UDI: 191072241252 Expiration Date: 1/6/2027
30 units
Z-3003-2026
American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H; Lot Code: Lot Number: 70-054952 UDI: 191072219947
12 units
Based on the official FDA remedy
What to do — step by step
Check Kit Details
Look for model number TNCB10AN, lot code 42-8768511, and expiration date January 6, 2027 on the kit.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 2 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of IA, OH.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Iowa, Ohio.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
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-3001-2026 (June 29, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3001-2026 to see it in context.
Plain-language summary written by qwen3:4b on September 14, 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.