# FDA recall Z-0645-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-10-09.

## Product

MEDLINE convenience kits labeled as:   1) C-SECTION OR 30 CDS, REF CDS820075V;  2) C-SECTION OR 30 CDS, REF CDS820075W;  3) C-SECTION, REF CDS980774M;  4) C-SECTION KIT, REF CDS981322AB;  5) C-SECTION KIT, REF CDS981322AC;  6) C-SECTION COMBINED CDS, REF CDS982398I;  7) C-SECTION PROCEDURE, REF CDS983450L;  8) C-SECTION-LF, REF CDS983869J;  9) C-SECTION, REF CDS984261J;  10) C-SECTION CDS-LF, REF CDS984516L;  11) C-SECTION CDS-LF, REF CDS984516M;  12) C-SECTION, REF CDS984902K;  13) C-SECTION, REF CDS984902L;  14) C-SECTION CDS, REF CDS985282F;  15) C-SECTION CDS, REF CDS985326G;  16) C SECTION, REF CDS985505G;  17) C-SECTION, REF CDSCCR611Q;  18) C-SEC GERBERUNI PK RFID-LF, REF DYNJ0100978K;  19) C-SECTION PACK-LF, REF DYNJ0101147G;  20) BR C-SECTION-LF, REF DYNJ0101562I;  21) BR C-SEC RFID-LF, REF DYNJ0101562K;  22) LUD C-SEC RFID-LF, REF DYNJ0101616L;  23) C-SECTION PACK-LF, REF DYNJ0173422AF;  24) C-SECTION PACK-LF, REF DYNJ0173422AG;  25) C-SECTION PACK-LF, REF DYNJ0190625Q;  26) 

## Reason for recall

Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0645-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-09
- **Report date:** 2024-12-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0645-2025

## Citation

> AI Analytics. FDA recall Z-0645-2025. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-0645-2025. Source: US FDA. Licensed CC0.

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