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fda medwatch·15h ago·1 min read
save

AVID Medical issues correction for convenience kits containing recalled Huons sodium chloride ampules

Sep 21, 2026·read at fda medwatch ↗RegulatoryNegative

AVID Medical has released a correction notice for certain convenience kits that include sodium chloride ampules from Huons Co., which are subject to a recall.

The FDA has classified this recall as the most serious type, indicating a risk of serious injury or death if the kits are used without correcting the affected components. AVID advises customers to correct the kits by removing the recalled ampules before further use, rather than removing the devices from service.

The notice lists specific kit models and lot numbers affected, including continuous nerve block trays, single shot epidural trays, basic biopsy trays, and universal imaging biopsy trays. Customers should follow the correction instructions provided by AVID to ensure safety.

source

This writeup was produced by pharmadog from original reporting by fda medwatch.

Original headline: “Convenience Kit Correction: AVID Medical Issues Correction for Kits Containing Huons Sodium Chloride Ampules”

read at fda medwatch ↗
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companies & drugs in this story

companies
UNIQUE
drugs
RNS-6011SODIUM CHLORIDE10LIDOCAINElidocaine SR
topics
Recall10

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