Fresh Recalls

FDAClass II · Medical device · Recall Z-2782-2026 · Recalled July 29, 2026

Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16 recall — Medline Industries, LP

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16
Company / brand
Medline Industries
Lot / serial / date codes
DYNJT6105 UDI-DI 10198459539381 Lots 25JBM474 25LBS203
Distribution
US Nationwide distribution in the states of CA, FL, MD. PA, and TX.
Agency product description and boundaries

Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. NON MB DAVINCI LITHOTOMY SM PK DYNJT6105

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16

3. Open the official notice or contact

Official recall ID
Z-2782-2026
Brand
Medline Industries
Classification
Class II
Units affected
980 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Northfield, IL, United States
Firm address
3 Lakes Dr, N/A, 60093-2753

Identifying details (verbatim from the notice)

Product codes / lots
DYNJT6105 UDI-DI 10198459539381 Lots 25JBM474 25LBS203
Distribution
US Nationwide distribution in the states of CA, FL, MD. PA, and TX.
Firm notified the public via
Letter
FDA event ID
99301
Recall initiated
June 8, 2026
FDA classified
July 23, 2026
FDA report date
July 29, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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