Medical Action Industries, Inc. 306 recalls
16 recalls in our records from 2020 to 2026: 16 FDA medical devices.
Recalls with full detail pages
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Medical Action Industries, Inc. 306 medical device recall: Kit: Epidural/Pain TQC 20/Cs
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
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Medical Action Industries, Inc. 306 medical device recall: Pack Angiography NCMC 3/Cs BANNER
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced…
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Medical Action Industries, Inc. 306 medical device recall: Medical Action Industries Inc. Pack Cath BHH
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and…
Earlier and other recalls
These link to the official agency notice.
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Medical Action Industries, Inc. 306 medical device recall: Generic Name: Kit Official notice ↗
An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.
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Medical Action Industries, Inc. 306 medical device recall: Blood Culture Collection Venipuncture Kit 20/Cs Official notice ↗
Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise…
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Medical Action Industries, Inc. 306 medical device recall: Brand Name: Medical Action Industries Product Name: Dialysis Change… Official notice ↗
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
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Medical Action Industries, Inc. 306 medical device recall: Foam Protective Pouches Official notice ↗
The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code.…
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Medical Action Industries, Inc. 306 medical device recall: IV Start Kit Official notice ↗
The kits contain saline flush syringes which were recalled by the supplier.
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Medical Action Industries, Inc. 306 medical device recall: Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D Official notice ↗
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Medical Action Industries, Inc. 306 medical device recall: Medical Action Industries Inc. Disposable Instrument Pack Official notice ↗
Scissors contained debris.
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Medical Action Industries, Inc. 306 medical device recall: Medical Action Industries Inc. Port Access Kit Official notice ↗
The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
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Medical Action Industries, Inc. 306 medical device recall: B. Braun CARESITE Port Access Kit w/Tegaderm Official notice ↗
The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
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Medical Action Industries, Inc. 306 medical device recall: Kit: Central Line Dres Change 20/Cs Official notice ↗
The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.
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Medical Action Industries, Inc. 306 medical device recall: Medical Action INDUSTRIES INC Official notice ↗
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
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Medical Action Industries, Inc. 306 medical device recall: Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420 Official notice ↗
Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
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Medical Action Industries, Inc. 306 medical device recall: Medical convenience trays and kits Official notice ↗
The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.