Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0209-2015 — AMS 700 Series Inflatable Penile Prosthesis Accessory Kit (AMS 700 Line Accessory Kit), 72401850. Keith Needles are part of the AMS 700 Accessory Kit. In conjunction with the Furlow Insertion Tool (Furlow), the Keith Needles facilitate the passing of the pulling sutures through the glans to place

U.S. FDA — Device Enforcement · United States · 2014-10-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0209-2015
Date of alert
2014-10-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
American Medical Systems, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
861912018
Reported risk: AMS' supplier has issued a recall of certain lots of Lightning Bolt Keith needles supplied in AMS 700 Accessory Kits. Based on this, AMS is recalling AMS 700 Accessory Kits which contain these lots of needles. The supplier made the decision to issue this recall after an internal investigation that was requested by AMS. The investigation identified a potential nonconformity that may lead to a bent or broken Keith Needle when used with the Furlow tool.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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