Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
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 manifold"
Read the official notice →- Date
- 2026-05-13
- Country
- United States
- Brand
- Medical Action Industries
- Product
- Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
- Classification
- Class I
- Units
- US distribution to state of: AZ OUS: None
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Medical Action Industries recalls
- 2026-09-16
USMedical Action Industries, Inc. 306 recalls Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride…
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
FDA · DeviceMedical Action Industries, Inc. 306US distribution to states of: IA, VA, MO, KS, FL, OH and LS.Official notice →- 2026-08-12
- US
Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the state of CA.Official notice → - 2026-08-05
- US
Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
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 into blood circulation and become lodged within…
- 2024-09-18
- US
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…
The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to…
FDA · DeviceMedical Action Industries, Inc. 306Nationwide distribution. International distribution to Canada.Official notice → - 2024-04-03
- US
Medical Action Industries, Inc. 306 recalls IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
The kits contain saline flush syringes which were recalled by the supplier.
FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the states of MN and ND. There as no…Official notice → - 2022-12-28
- US
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box,…
Scissors contained debris.
FDA · DeviceMedical Action Industries, Inc. 306Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no…Official notice →
Other drugs & medical recalls in the United States
- 2026-05-13
- US
Centinel Spine, Inc. recalls Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.
Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.
FDA · DeviceCentinel Spine, Inc.US Nationwide distribution in the states of AZ, CA, GA, LA, MO, NY, TN, TX.Official notice → - US
Boston Scientific Corporation recalls LUX-DX II, Arrythmia detector and alarm, Model M302, with SERVER SW LATITUDE DRAGON US, Model 6460, Version 7.5
For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for Bradyarrhythmia and Pause (M312 only). In…
FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the country of Belgium.Official notice → - US
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS4200 Software…
Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.
FDA · DeviceIntuitive Surgical, Inc.Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice → - US
American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers…
Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential…
FDA · DeviceAmerican Contract Systems IncUS distribution to MN. No OUS distribution.Official notice → - US
AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- US
Ventec Life Systems, Inc. recalls VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000
Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could…