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

Recall Z-1369-2018 — Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 (c) 650704160 551316 Product Usage: RUSCH Simplastic Suprapubic Puncture Instruments are indicated for emergency suprapubic drainage of the bladder.

U.S. FDA — Device Enforcement · Ireland · 2018-03-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1369-2018
Date of alert
2018-03-15
Country / jurisdiction
Ireland
Risk level
Class II
Risk type
recall
Brand
Teleflex Medical Europe Ltd
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
650704100
Reported risk: These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.