Karl Storz Endoscopy recalls Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10

Recalled May 20, 2020 · FDA recall Z-1942-2020 · Karl Storz Endoscopy

Hazard

The sterile single-use tubing may contain higher ethylene oxide (EO) residues than the acceptable level. · FDA Class III

Units

543 boxes were distributed; 10 ea per box.

Sold at

57 consignees in the US. AL,AZ,CA,CT,DE,FL,GA,IL,LA,MA,MD,ME,MI,MN,NE,NH,NJ,NY,OH,OK,PA,SC,TX,VA,VT,WA and WI

Description

The sterile single-use tubing may contain higher ethylene oxide (EO) residues than the acceptable level.

Product

Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10

Manufacturer(s)

Karl Storz Endoscopy

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →