BfArM - Federal Institute for Drugs and Medical Devices

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Product group ophthalmological technology
Reference 01559/08

Recall of the Bausch & Lomb Non-Sterile multiple-use Phaco Needles (article numbers see annex). The non-sterile products are recalled because of the wrong use of “sterile” and “non-reuse” symbols in the Instructions for Use. The firm has evaluated the product related patient risk to be low.

Recall Phaco Needles, Bausch & Lomb , Download_VeroeffentlichtAm_EN PDF, 75KB, File does not meet accessibility standards