MicroAire PAL¿ Cannula Product Usage - Power Aspiration recall
MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
Why was MicroAire PAL¿ Cannula Product Usage - Power Aspiration recalled?
MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del Vecchio French Rasp cannula), due to our receipt of three (3) complaints that it bent or broke during surgery. Accordingly, the PAL-R4011XL has also been put on production hold until further notice.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Include lot numbers/serial numbers 0913228216, 0414243005, 0215266350, 0415269875, 0515271334
- Product
- MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
- Recalling firm
- MicroAire Surgical Instruments, LLC
- Quantity
- 145 manufactured and distributed
- Distribution
- Worldwide Distribution - US Nationwide
- Recall date
- April 13, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)