Reported Jan 15, 2020 · Terminated
Medical convenience trays and kits, labeled as
Medical Action Industries, Inc. 306
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medical Action Industries, Inc. 306 · 25 Heywood Road · Arden, NC · 28704-9302
Is this the product you have?
63 of 63 products
| Model / number | Product as published |
|---|---|
77070B | — |
| — | Lot Numbers: 0000250140 0000250814 0000251345 0000252860 0000253786 0000254661 0000255539 0000256372 0000256478 0000256896 0000257916 0000259710 0000260807 0000261950 0000262411 0000262853 0000263255 0000248930 0000248004 0000245391 ***DIALYSIS*** Clear Sequence Change Kit |
77068B | — |
| — | Lot Numbers: 0000255949 0000256795 0000258076 0000260410 0000261183 0000262656 0000257187 ***PEDS CVC*** Clear Sequence Change Kit |
77190B | — |
| — | Lot Numbers: 0000261186 0000261949 0000263402 0000245684 ***PICC*** Clear Sequence Change Kit |
77069B | — |
| — | Lot Numbers: 0000250126 0000250752 0000251646 0000252449 0000255455 0000256371 0000256796 0000256897 0000257625 0000258163 0000260908 0000262404 0000262852 0000249190 0000248773 Adult Central Line Dressing Change Kit |
74636C | — |
| — | Lot Numbers: 0000250172 0000251684 0000251775 0000252730 0000255062 0000255669 0000256289 0000257970 0000259210 0000259867 0000260734 0000263279 0000264415 0000248260 Central Line Dressing Kit, VCU |
57647B | — |
| — | Lot Numbers: 0000249224 0000248261 Central Line Removal Kit |
78631B | — |
| — | Lot Numbers: 0000258405 0000264395 Chest Tube Cleaning Kit |
73000 | — |
| — | Lot Numbers: 0000254875 0000256642 0000257028 0000261394 0000248107 0000247565 0000246033 0000244487 CVC Dressing Change Kit |
80643D | — |
| — | Lot Numbers: 0000263867 Dressing Change Kit |
71538 | — |
| — | Lot Numbers: 256205 0000256888 ED Suture Set |
- Amount recalled
- 9924 cases
Where it was sold
Why it was recalled
The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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