Reported Dec 25, 2013 · Terminated
Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage:…
Kimberly-Clark Corporation
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: Kimberly-Clark Corporation · 1400 Holcomb Bridge Rd · Roswell, GA · 30076-2190
Is this the product you have?
- Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR
- Syringe (BD Code 405198) Product UsageThe device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs
- Lot codes and dates
- Lot numbers
181024181129 181217181221181231182022182058182101182108182131182222182223182263182265182289182293182301182315181A074181A94181A154181A177181A286181A289181A369182A002182A005182A012182A055182A056182A057182A064182A074182A075/182A78182A085182090182A142182AA144182A151182A155182A178182A194182A196182A198182A202182A204182A212182A216 and 189A001 (syringe)
- Lot numbers
- Amount recalled
- 389,300 units
Where it was sold
- Nationwide
Why it was recalled
Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7 mL Epilor plastic Luer-Lok LOR Syringes under recall by Becton Dickinson (BD) because the product may stall or stick when traveling within the barrel of the syringe.
This product could cause temporary or reversible health problems — stop using it.
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