← Every firm

Medical Action Industries, Inc. 306 FDA Recalls

24 recalls on file across devices, 10 of them Class I and 8 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product
Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture ColleClass IIJul 23, 2026Blood culture convenience kits contain a component subject t
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampulesClass IJul 23, 2026Kits containing Sodium Chloride ampules subject to another r
Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Class IJul 23, 2026Kits containing Sodium Chloride ampules subject to another r
Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791Class IIMay 21, 2026Convenience kits contain needle free access device that has
Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle ManifoldsClass IMay 13, 2026Cardiovascular procedure kits contain manifolds, the subject
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/CaseClass IMar 17, 2026Convenience kit contains a syringe in which the rotating ada
Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/Class IIJun 11, 2024The protective pouches were identified to have been improper
IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.Class IIJan 15, 2024The kits contain saline flush syringes which were recalled b
Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kitClass IINov 4, 2022XXX
Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/Class IIOct 12, 2022Scissors contained debris.
Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries IncClass IIOct 12, 2022The Port Access Kits were incorrectly labeled as IV Start Ki
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 1Class IISep 15, 2022The kits were incorrectly labeled with an extended expiratio
Kit: Central Line Dres Change 20/CsClass IISep 8, 2021The ChloraPrep 3ml kit component has a shorter expiry date t
Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214Class IIMay 11, 2021There is a potential for flaking metal and/or brown spots on
Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209Class IIMay 11, 2021There is a potential for flaking metal and/or brown spots on
Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224Class IIMay 11, 2021There is a potential for flaking metal and/or brown spots on
Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220Class IIMay 11, 2021There is a potential for flaking metal and/or brown spots on
novaplus, General Purpose Kit, Cat. No. 56603Class IIMay 11, 2021There is a potential for flaking metal and/or brown spots on
Kit: Blood Culture MAI Kit Part Number: 80076Class IApr 9, 2021Medical convenience kits are being recalled due to a potenti
Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420Class IApr 9, 2021Medical convenience kits are being recalled due to a potenti
Kit: Blood Culture. MAI Kit Part Number: 80315DClass IApr 9, 2021Medical convenience kits are being recalled due to a potenti
Kit: Injection REVIEW MAI Kit Part Number: 74736Class IApr 9, 2021Medical convenience kits are being recalled due to a potenti
Kit: Midline Insertion DA. MAI Kit Part Number: 77981BClass IApr 9, 2021Medical convenience kits are being recalled due to a potenti
Kit: LVAD Dres Chg. MAI Kit Part Number: 79544BClass IApr 9, 2021Medical convenience kits are being recalled due to a potenti

Related datasets