Leica Surgical Microscope Recall Due to Brake Failure During Installation
Leica Microsystems is recalling five surgical microscopes because the Z-axis and/or AB and C-axis brakes failed during installation.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II. The hazard involves a mechanical failure (brake failure) in a medical device used for human and veterinary treatment, which presents a risk of harm, but the source text does not report any specific injuries or illnesses.
Plain-English summary
Leica Microsystems (Schweiz) Ag is recalling five units of surgical microscopes. The devices are used to improve the visibility of objects through magnification and illumination for observation, documentation, and human or veterinary medical treatment.
The recall was initiated because the brake in the Z axis and/or brakes in the AB and C axes failed during installation. The affected units have serial numbers OH4-84712, OH4-84812, and OH4-84912.
The products were distributed worldwide, including nationwide in the United States (specifically AK, CA, CO, NY, and OR) and in Belarus, China, Hong Kong, India, Indonesia, Italy, Norway, South Africa, Spain, Sweden, Turkey, and Vietnam. Users should contact the recalling firm for further instructions.
The recalled product
- Product
- Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for observation and documentation and for human veterinary medical treatment.
- Manufacturer
- Leica Microsystems (Schweiz) Ag
- Affected units
- 5
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Serial Numbers: OH4-84712
- OH4-84812
- OH4-84912
Distribution
Part of a larger recall action
This product is one of 2 recalled by Leica Microsystems (Schweiz) Ag under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Leica Microsystems (Schweiz) Ag
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