Reported May 16, 2018 · Terminated
Connecting Tube - Female to Male Luer Lock, HPCT8.8-120-M-FM Product Usage: The connecting tube is intended to be a…
Cook Inc.
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: Cook Inc. · 750 N Daniels Way · Bloomington, IN · 47404-9120
Is this the product you have?
- Connecting Tube - Female to Male Luer Lock, HPCT8.8-120-M-FM
- Product UsageThe connecting tube is intended to be a conduit between a fluid reservoir and a vascular catheter in the patient. The connecting tube may be used during angiographic procedures to connect radiographic contrast power injector to a vascular catheter, arterial pressure monitoring, and fluid infusion
- Lot codes and dates
68 of 68 codes
Lots 779716478440387844039784404078440417844042784643478464357853869785387078538717853872785387378538747857491785749278574937857494785749578574967857497785749878574997857500786374278637447863745786374778637487863749786375078637517871644787164578716467871647788193778819387881939788194078819417881942788849878885057888506788850779174237917424791742579174267917434792513679251377925138792513979251407940326794032779403287940345
- Amount recalled
- 6345
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Cap-adapter assembly of the device may potentially not be adequately tightened, possibly leading to fluid leakage from or air aspiration into the connecting tube.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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