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Beaver Visitec

Complete recall history across all FDA and CPSC categories — 6 total recalls

Beaver Visitec appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (6)

FDA medical device enforcement actions by Beaver Visitec

Date Product Reason Class
Mar 12, 2019 Beaver Xstar Slit Knife 2.4 mm, 45degree Double Bevel, Ophthalmic-utilized i... Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double Bev... Class II
Feb 19, 2019 Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm... The product contains a misprinted expiration date on the peel pack. Both wer... Class III
Nov 30, 2018 BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Sof... Certain lots are missing a protective sheath component over the silicone tip,... Class II
Jul 19, 2018 Beaver Accu-Temp High Temperature Cautery, 2 inch Shaft with Fine Tip, Model ... A small number of devices in this lot may have a melted cap and a hole formed... Class II
Jun 18, 2018 Slit Knife 2.6mm 45degree Bevel Up, Model Number 373726. for use in ophthalmi... Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual ... Class II
May 14, 2018 Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to m... Blades are loose in handles and may fall out due to non cured epoxy Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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