medical MODERATE Updated 2021-04-07

Oscor, Inc. recalls AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 -

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Recalled Product

AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various types of pacing leads and catheters.

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Hazard / Issue

Potential for open seal on sterile product

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: GUDID: 25051684026298; Lot Number DP-11759

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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View official government recall

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