Medical convenience trays and kits — Class II medical device recall Z-0779-2020
Terminated recall by Medical Action Industries, Inc. 306, reported 2020-01-15, distributed in AZ, CA, FL, GA, IL, IN, KY, LA…. The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
| Recall number | Z-0779-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Action Industries, Inc. 306, Arden, NC, United States |
| Recall initiated | 2019-12-02 |
| Classified | 2020-01-06 |
| Reported by FDA | 2020-01-15 |
| Terminated | 2023-01-24 |
| Distributed | AZ, CA, FL, GA, IL, IN, KY, LA, MA, MD, MI, MO, NC, NE, OH, PA, RI, SC, TX, VA, WA |
| Quantity | 9,924 cases |
| Lot numbers | 0000244487CVC, 0000245391, 0000245684, 0000246033, 0000247565, 0000247839, 0000248004, 0000248107, 0000248176, 0000248259, 0000248260, 0000248261, 0000248262, 0000248306, 0000248502, 0000248773, 0000248930, 0000249190, 0000249224, 0000249687, 0000250126, 0000250140, 0000250172, 0000250752, 0000250772, 0000250813, 0000250814, 0000250817, 0000250818, 0000250819, 0000250820, 0000251345, 0000251646, 0000251684, 0000251690, 0000251775, 0000252258, 0000252449, 0000252599, 0000252601 and 153 more |
| Model numbers | 4129, 56791B, 56957, 57647B, 57888B, 59299C, 59387, 59387B, 59589C, 59806B, 59836, 68330, 68358, 69477B, 71538, 71538ED, 71582, 72347, 72347B, 73000, 73000CVC, 74635C, 74636C, 75378, 77068B and 7 more |
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 Suture Kit, REF 59836 Trach Care Kit, Kit de Traqueostomia, REF LH_68162B Trach Care Tray, REF 56791B Trach Care Tray, REF 75378 Tracheostomy Care Tray, REF 4129 Tracheostomy Tray, REF 80209 Wound Care Kit, REF 68330 Wound Care Tray, REF 68358 MEDICHOICE: Tracheostomy Kit, Reorder: TRAC1002 THERAPY SUPPLY HOUSE: VAD DRESSING CHANGE KIT, Reorder # 76512B
Reason for recall
The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0779-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.