RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0
Reported: June 5, 2019 Initiated: April 1, 2019 #Z-1682-2019
Product Description
RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0
Reason for Recall
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 1787 units
- Distribution
- Nationwide
- Location
- Morrisville, NC
Frequently Asked Questions
What product was recalled? ▼
RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0. Recalled by Teleflex Medical. Units affected: 1787 units.
Why was this product recalled? ▼
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 5, 2019. Severity: Moderate. Recall number: Z-1682-2019.
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