Reported Sep 12, 2012 · Terminated
100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to ethylene oxide…
Steris Corporation
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.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: Steris Corporation · 5960 Heisley Rd · Mentor, OH · 44060-1834
Is this the product you have?
- 100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to ethylene oxide sterilization. Tube maintains sterility of the enclosed medical devices until opened.
- Lot codes and dates
- Product code KCT
- Lot number60263
- Amount recalled
- 77 packs
Where it was sold
Why it was recalled
On 7/20/2012 the firm became aware that a lot of tubing was distributed by the supplier after it was rejected by Steris due to failing process indicators.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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