# FDA recall Z-2940-2020

> **Medical Components, Inc dba MedComp** · Class II · device recall initiated 2020-07-27.

## Product

Medcomp 15.SF X 24CM Titan HD CATHETER  (CUFF 19CM FROM TIP)  Ref: THD155024

## Reason for recall

Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer

## Distribution

AZ, CA. FL. GA, NC, ND, NJ, NY, OH, PA, VA, WA

## Key facts

- **Recall number:** Z-2940-2020
- **Recalling firm:** Medical Components, Inc dba MedComp
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-27
- **Report date:** 2020-09-16
- **Termination date:** 2021-04-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Harleysville, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2940-2020

## Citation

> AI Analytics. FDA recall Z-2940-2020. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2940-2020. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
