Lower risk Medical device recall · FDA · Published December 2, 2019

Medical Action Industries CVC Clear Sequence Change Kits May Have Saline pH Issues

Medical Action Industries recalls certain CVC Clear Sequence Change Kits due to saline solution pH potentially exceeding USP standards (4.5-7.0). Affected kits include specific models and lot numbers listed in the recall notice.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0779-2020Medical device Medical Action Industries ›

Lower-risk recall

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

Take action

Contact the company

Recalling firmMedical Action Industries, Inc. 30625 Heywood Road · Arden, NC 28704-9302

✎ GovInfoNow plain-language explainer

Medical Action Industries is recalling several types of medical convenience trays and kits, including CVC Clear Sequence Change Kits, because the saline solution inside may have a pH outside the safe range (4.5-7.0) as per USP standards. This could potentially cause issues with medical treatments. Read more at govinfonow.com/recall/66416-medical-action-industries-cvc-clear-sequence-change-kits-may-have.

Source Summary by GovInfoNow · govinfonow.com/recall/66416-medical-action-industries-cvc-clear-sequence-change-kits-may-have · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0779-2020

Cite this page

“Medical Action Industries CVC Clear Sequence Change Kits May Have Saline pH Issues.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66416-medical-action-industries-cvc-clear-sequence-change-kits-may-have. Based on FDA recall #Z-0779-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0779-2020%22&limit=1).

The FDA announced on December 2, 2019, that Medical Action Industries is recalling medical convenience trays and kits due to saline solution bottles that may exceed USP pH requirements. The agency issued recall number Z-0779-2020 for the Class II voluntary recall.

How to tell if you have it

Brand: Medical Action Industries
Product: *CVC* Clear Sequence Change Kit, REF 77070B
Product: *DIALYSIS* Clear Sequence Change Kit, REF 77068B
Product: *PEDS CVC* Clear Sequence Change Kit, REF 77190B
Product: *PICC* Clear Sequence Change Kit, REF 77069B
Product: Adult Central Line Dressing Change Kit, REF 74636C
Product: Central Line Dressing Kit, VCU, REF 57647B
Product: Central Line Removal Kit, REF 78631B
Product: Chest Tube Cleaning Kit, REF 73000
Product: CVC Dressing Change Kit, REF 80643D
Product: Dressing Change Kit, REF 71538
Product: ED Suture Set, REF 59299C
Product: Laceration Kit, REF 59806B
Product: Laceration Tray, REF 56957
Product: Laceration Tray, REF 57888B
Product: Laceration Tray, REF 59387
Product: Laceration Tray, REF 59387B
Product: Laceration Tray, REF 69477B
Product: Laceration Tray, REF 71582
Product: LACERATION/SUTURE REMOVAL, REF 72347
Product: LACERATION/SUTURE REMOVAL, REF 72347B
Product: Pediatric Central Line Dressing Kit, REF 74635C
Product: PICC Central Line Dressing Kit VCU, REF 59589C
Product: PICC/CVC/Central /Dialysis Clear Sequence Dressing Kit, REF 78197
Product: Suture Kit, REF 59836
Product: Trach Care Kit, Kit de Traqueostomia, REF LH_68162B
Product: Trach Care Tray, REF 56791B
Product: Trach Care Tray, REF 75378
Product: Tracheostomy Care Tray, REF 4129
Product: Tracheostomy Tray, REF 80209
Product: Wound Care Kit, REF 68330
Product: Wound Care Tray, REF 68358
Brand: MEDICHOICE
Product: Tracheostomy Kit, Reorder: TRAC1002
Brand: THERAPY SUPPLY HOUSE
Product: VAD DRESSING CHANGE KIT, Reorder # 76512B

The hazard

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

Context

GovInfoNow's records show Medical Action Industries, Inc. 306 has 15 other recalls on record since April 9, 2021. Other recent recalls include a July 23, 2026 recall of Blood Culture Kits for risk of localized infection due to packaging seals and an Epidural Pain Kit recall for potentially compromised sterility. On January 7, 2026, Medline Convenience Kits were recalled for the risk of contaminated sterile products.

How to tell if you have this one

Check for the product names listed in the recall, such as 'CVC Clear Sequence Change Kit', 'Dialysis Clear Sequence Change Kit', and others. Look for specific lot numbers like 0000250140 or 0000250814 on the packaging.

Brand
Medical Action Industries
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the product name and lot number on the packaging to confirm if it's affected by this recall.

Where it went and when

Where it was distributed

Distributed in 21 states.

FDA distribution: “MA, RI, PA, MD, VA, NC, SC, GA, FL, KY, OH, IN, MI, IL, MO, NE, LA, TX, AZ, CA, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Missouri, Nebraska, North Carolina, Ohio, Pennsylvania, Rhode Island, South Carolina, Texas, Virginia, Washington.

Recall timeline

FDA terminated this recall 3.1 years after the firm started it.

Dec 2, 2019Firm started the recall
Jan 6, 2020FDA classified it Class II
Jan 15, 2020Published in FDA’s Enforcement Report
Jan 24, 2023FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

How can I find out if my kit is in the recall?

Check the product name and lot number on the packaging against the list of affected products and lot numbers provided in the recall notice.

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Link to this recall

<a href="https://govinfonow.com/recall/66416-medical-action-industries-cvc-clear-sequence-change-kits-may-have">Medical Action Industries CVC Clear Sequence Change Kits May Have Saline pH Issues (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0779-2020 (December 2, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0779-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.