medical MODERATE Updated 2018-04-04

Teleflex Medical recalls Teleflex MEDICAL WECK Visistat 35. Used for the external sk

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Recalled Product

Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.

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Hazard / Issue

Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.

Issued by

FDA

Affected States: KS
Lot/Code Info: Lot Number 73H1600207

✅ 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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Search Amazon for Teleflex MEDICAL WECK Visistat →

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