Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate. These products are used in all sections of the eye. This cannula is a general use cannula mainly designed for the precise maintenance of optimum anterior chamber depth
Reported: June 4, 2014 Initiated: May 6, 2014 #Z-1664-2014
Product Description
Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate. These products are used in all sections of the eye. This cannula is a general use cannula mainly designed for the precise maintenance of optimum anterior chamber depth
Reason for Recall
Contains a sharp tip needle when the product should contain a blunt tip cannula
Details
- Recalling Firm
- Beaver-Visitec International Inc.
- Units Affected
- 9970 units
- Distribution
- Nationwide Distribution including AL, CT, IN, NC, NY, TX, and VA.
- Location
- Waltham, MA
Frequently Asked Questions
What product was recalled? ▼
Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate. These products are used in all sections of the eye. This cannula is a general use cannula mainly designed for the precise maintenance of optimum anterior chamber depth. Recalled by Beaver-Visitec International Inc.. Units affected: 9970 units.
Why was this product recalled? ▼
Contains a sharp tip needle when the product should contain a blunt tip cannula
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 4, 2014. Severity: Moderate. Recall number: Z-1664-2014.
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