Medical Action Industries, Inc. 306 recalls
Every recall we track for Medical Action Industries, Inc. 306 — 26 in all, from 2019–2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Medical Action Industries, Inc. 306 peaked in 2021 (12); 26 since 2017. 8% rated “stop using now”.
All FDA recall records for Medical Action Industries, Inc. 306 since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 12 | 0 | 12 |
| 2022 | 0 | 0 | 3 | 1 | 4 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 1 | 1 | 2 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 2 | 1 | 4 | 0 | 7 |
What to do if you have a recalled Medical Action Industries, Inc. 306 product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Medical Action Industries, Inc. 306 recalls
16 shown- Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture
Medical Action Industries recalls blood culture kits with potential packaging seal issues that could cause skin or soft tissue infections if used. Affected kits include specific model numbers and dates.
Medical Action IndustriesJul 23, 2026 - Stop using nowMedical device
Medical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Recalled Medical Action Industries Epidural/Pain TQC 20/Cs kits with Sodium Chloride 0.9% ampules may have compromised sterility. Affected lots expire through 2027. Stop using immediately.
Medical Action IndustriesJul 23, 2026 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot
Medical Action Industries recalls 4,000 units of Urinary Clean Catch Kit (Lot 333606) with an incorrect expiration date of March 31, 2027 instead of February 28, 2027.
Medical Action IndustriesJul 9, 2026 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Recall of Medical Action Industries Dialysis Change Tray Clear Sequence model 78791 due to improper silicone seal that may cause doming or tearing. Affected units sold with specific lot codes.
Medical Action IndustriesMay 21, 2026 - Stop using nowMedical device
Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
Medical Action Industries recalls Pack Angiography NCMC 3/Cs BANNER kits with Medline Namic Angiographic Star Off Handle Manifolds due to potential particulate in fluid paths that could enter blood circulation.
Medical Action IndustriesMay 13, 2026 - Use cautionMedical device
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Recall of 5-unit medical catheter kits with potential syringe disconnection risk. Affected units have specific lot numbers and reference codes.
Medical Action IndustriesMar 17, 2026 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75
Medical Action Industries recalls foam protective pouches with incorrect GMDN codes due to mislabeled UDI. Affected models include 6010, 6010-1, 6060, and others. No immediate action required as the hazard is a labeling error.
Medical Action IndustriesJun 11, 2024 - UnratedMedical device
Medical Action Industries, Inc. 306 recalls IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Recalled Medical Action Industries IV Start Kits (100 kits/case) with saline syringes from specific lot numbers. These kits were recalled by the supplier due to potential safety issues.
Medical Action IndustriesJan 15, 2024 - UnratedMedical device
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
Medical Action Industries recalls cardiac catheter introduction kits with REF 58647D. Affected units have specific lot numbers and UDI/DI codes. Consumers should contact the manufacturer for details.
Medical Action IndustriesNov 4, 2022 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20
Recall of 20-pack disposable scissors with debris. Stop using if you have these sterile medical instruments.
Medical Action IndustriesOct 12, 2022 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries
Medical Action Industries recalls Port Access Kits with incorrect IV Start Kit labeling. This labeling error may cause confusion in medical use. Affected kits have specific lot numbers and expiration dates.
Medical Action IndustriesOct 12, 2022 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected
Recall of B. Braun CARESITE Port Access Kit w/Tegaderm with incorrect expiration date. Products labeled with extended expiration date of 02/21/2024 instead of 02/10/2024.
B. BraunSep 15, 2022 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Kit: Central Line Dres Change 20/Cs
Recall of Central Line Dressing Kit 20/Cs with shorter expiry date than labeled. Affected units expire 03/31/2024. No immediate action needed but check expiration dates.
Medical Action IndustriesSep 8, 2021 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls novaplus, General Purpose Kit, Cat. No. 56603
Medical Action Industries recalls novaplus hemostats with potential flaking metal or brown spots. Affected kits have batch numbers 0000275724 (exp 02/15/2022) and 0000277619 (exp 04/15/2022).
Medical Action IndustriesMay 11, 2021 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B
Medical Action Industries recalls LVAD dressing change kit (part 79544B) due to potential breach in BD ChloraPrep 3mL applicator packaging. Affected units were sold with specific lot numbers and expiration dates.
Medical Action IndustriesApr 9, 2021 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit,
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.
Medical Action IndustriesDec 2, 2019
Medical Action Industries, Inc. 306 recall questions
How many recalls has Medical Action Industries, Inc. 306 had?
26 recalls from Medical Action Industries, Inc. 306 are on record with U.S. safety agencies, from 2019–2026.
What is the most recent Medical Action Industries, Inc. 306 recall?
Medical Action Industries, Inc. 306 recalls Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture, dated Jul 23, 2026. Every Medical Action Industries, Inc. 306 recall is listed on this page, newest first.
What should I do if I have a recalled Medical Action Industries, Inc. 306 product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Medical Action Industries, Inc. 306 recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.