FDA Classifies Baxter's Removal Of Certain Duo-Vent Solution Set Lots As Class I Recall Over Air Bubble Risk; Baxter Says No Serious Injuries Or Deaths Reported
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Why It Matters
Baxter had to recall some medical equipment because of a problem with air bubbles that could be dangerous. When a company fixes a safety issue fast and nobody got hurt, it shows they're being careful, so watch if they handle it well.
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Source: Benzinga · Read the original report at the publisher. Headline and figures shown for context; data may be delayed.
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