Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Reported: April 4, 2018 Initiated: February 15, 2018 #Z-1193-2018
Product Description
Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Reason for Recall
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.
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 12 units
- Distribution
- KS
- Location
- Research Triangle Park, NC
Frequently Asked Questions
What product was recalled? ▼
Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.. Recalled by Teleflex Medical. Units affected: 12 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 4, 2018. Severity: Moderate. Recall number: Z-1193-2018.
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