# FDA recall Z-0779-2020

> **Medical Action Industries, Inc. 306** · Class II · device recall initiated 2019-12-02.

## Product

Medical convenience trays and kits, labeled as:    Medical Action Industries, Inc.:  ***CVC*** Clear Sequence Change Kit, REF 77070B  ***DIALYSIS*** Clear Sequence Change Kit, REF 77068B  ***PEDS CVC*** Clear Sequence Change Kit, REF 77190B  ***PICC*** Clear Sequence Change Kit, REF 77069B  Adult Central Line Dressing Change Kit, REF 74636C  Central Line Dressing Kit, VCU, REF 57647B  Central Line Removal Kit, REF 78631B  Chest Tube Cleaning Kit, REF 73000  CVC Dressing Change Kit, REF 80643D  Dressing Change Kit, REF 71538  ED Suture Set, REF 59299C  Laceration Kit, REF 59806B  Laceration Tray, REF 56957  Laceration Tray, REF 57888B  Laceration Tray, REF 59387  Laceration Tray, REF 59387B  Laceration Tray, REF 69477B  Laceration Tray, REF 71582  LACERATION/SUTURE REMOVAL, REF 72347  LACERATION/SUTURE REMOVAL, REF 72347B  Pediatric Central Line Dressing Kit, REF 74635C  PICC Central Line Dressing Kit VCU, REF 59589C  PICC/CVC/Central /Dialysis Clear Sequence Dressing Kit, REF 78197  Su

## Reason for recall

The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.

## Distribution

MA, RI, PA, MD, VA, NC, SC, GA, FL, KY, OH, IN, MI, IL, MO, NE, LA, TX, AZ, CA, WA

## Key facts

- **Recall number:** Z-0779-2020
- **Recalling firm:** Medical Action Industries, Inc. 306
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-02
- **Report date:** 2020-01-15
- **Termination date:** 2023-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arden, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0779-2020

## Citation

> AI Analytics. FDA recall Z-0779-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0779-2020. Source: US FDA. Licensed CC0.

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