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Class IIOngoing

American Contract Systems Inc recalls 4 products

Recall date · record updated Sep 2, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
American Contract Systems Inc
Reason
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. 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.
Hazard
FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).
Who’s affected
US Nationwide distribution in the states of IA, OH.
Where
Nationwide
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99514…

Products (4)

  1. American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM

    Codes/lots: Lot Code: Lot Number: 42-8493811 UDI: 191072232991 Expiration Date: 7/15/2026Quantity: 30 unitsRecall no. Z-3000-2026Class II

  2. American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN

    Codes/lots: Lot Code: Lot Number: 42-8768511 UDI: 191072239907 Expiration Date: 1/6/2027Quantity: 30 unitsRecall no. Z-3001-2026Class II

  3. American Contract System Convenience Kits, CV B PACK, Model/Catalog Number: TNCB10AP

    Codes/lots: Lot Code: Lot Number: 42-8808611 UDI: 191072241252 Expiration Date: 1/6/2027Quantity: 30 unitsRecall no. Z-3002-2026Class II

  4. American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H

    Codes/lots: Lot Code: Lot Number: 70-054952 UDI: 191072219947Quantity: 12 unitsRecall no. Z-3003-2026Class II

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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