Reported Apr 18, 2018 · Terminated

Simplastic Suprapubic Puncture Instruments

Teleflex Medical Europe Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Teleflex Medical Europe Ltd · Ida Business Park · Athlone · N/A

Is this the product you have?

Simplastic Suprapubic Puncture Instruments

3 of 3 products

Products covered by this recall
Model / numberProduct as published
551310Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100
551312(b) 650704120
551316(c) 650704160
Lot codes and dates
  • Product Code Equivalent
  • Code (a) 650704100 551310 Batch Numbers13HE35 14KE45 (b) 650704120 551312
  • Batch Numbers
    • 13EE20
    • 13HE35
    • 13JE43
    • 14AE02
    • 14BE07
    • 14EE21
    • 14GE29
    • 14IE39
    • 15AE03
    • 15HE32
    (c) 650704160 551316
  • Batch Numbers
    • 13GE31
    • 13HE35
    • 13JE41
    • 13JE42
    • 13JE43
    • 13KE48
    • 14AE03
    • 14BE07
    • 14CE11
    • 14DE17
    • 14DE18
    • 14EE21
    • 14EG21
    • 14GE28
    • 14HE33
    • 14HE35
    • 14IE39
    • 14KE45
    • 15AE03
    • 15EE20
    • 15EE22
    • 15GE28
    • 15JE43
    • 15JE44
    • 13EG28
    • 13HG23
Amount recalled
4220 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Teleflex Medical Europe Ltd. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 5, 2020 · Data as of Sep 19, 6:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.