Tag: spectra_medical_devices

FDA Flags Class I Recall as Spectra Medical Pulls Sodium Chloride Flush Ampules

18 Sep 2026 2:42 p.m. · Source: US Food and Drug Administration

Spectra Medical Devices is removing Sodium Chloride Flush products made by Huons Co., Ltd. after an FDA inspection found quality issues. The recall is Class I, the most serious type.

Health Business Law Enforcement Medical Science Legal USA Product Recall Sodium Chloride Flush Spectra Medical Devices Huons Co., Ltd.FDA Class I Recall Sodium Chloride Injection USP Food Recalls Drugs
FDA Issues Early Alert for AVID Medical Kits Containing Recalled Sodium Chloride

2 Sep 2026 1:25 p.m. · Source: US Food and Drug Administration

AVID Medical convenience kits contain recalled sodium chloride ampules, raising sterility and quality concerns. The FDA issued an "Early Alert" due to potential risks of infection and severe complications, especially for critically ill patients and spinal procedures.

Health Business Science & Technology Medical Science Legal Education AVID Medical Sodium Chloride Medical Device Recall FDA Huons Co., Ltd.Spectra Medical Devices Epidural Kits Food Recalls Drugs