Recall Z-1088-2019— Beaver Visitec
Class III · Terminated
Class III FDA medical device recall by Beaver Visitec, initiated 2019-02-19, terminated 2020-07-21. FDA's recall record names no specific 510(k) clearance for this event. Product: Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. .. Reason: The product contains a misprinted expiration date on the peel pack. Both were printed as "180615", which is the lot number. The Lot number is correct..
- Recalling firm
- Beaver Visitec
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2019-02-19
- Terminated
- 2020-07-21
- Firm location
- Waltham, MA, United States
Product description
Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. .
Reason for recall
The product contains a misprinted expiration date on the peel pack. Both were printed as "180615", which is the lot number. The Lot number is correct.
Data sourced from openFDA. This site is unofficial and independent of the FDA.