Home / Recalls / Beaver Visitec / Z-2740-2018

Z-2740-2018 Class II Terminated

Recalled by Beaver Visitec — Waltham, MA

FDA device recall Z-2740-2018 was initiated by Beaver Visitec on June 18, 2018 and is designated Class II. Reason for recall: Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual packages within the correctly labeled shelf carton. The recall status is terminated (terminated October 30, 2019). Affected quantity: 440.

Recall Details

Product Type
Devices
Report Date
August 15, 2018
Initiation Date
June 18, 2018
Termination Date
October 30, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
440

Product Description

Slit Knife 2.6mm 45degree Bevel Up, Model Number 373726. for use in ophthalmic surgery.

Reason for Recall

Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual packages within the correctly labeled shelf carton.

Distribution Pattern

Distribution to US states of CA, IL, MD, MN, NJ, OH & PA; and Israel

Code Information

Lot Number 6001700

Other recalls by Beaver Visitec

  • Z-1111-2019 Class II — Beaver Xstar Slit Knife 2.4 mm, 45degree Double Bevel, Ophthalmic-utilized in C (March 12, 2019)
  • Z-1088-2019 Class III — Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30 (February 19, 2019)
  • Z-1066-2019 Class II — BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft T (November 30, 2018)
  • Z-3045-2018 Class II — Beaver Accu-Temp High Temperature Cautery, 2 inch Shaft with Fine Tip, Model Num (July 19, 2018)
  • Z-2342-2018 Class II — Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make (May 14, 2018)

FDA data resources