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LumiraDx recalls SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample collection in the intended nasal area. Cata
Recalled June 21, 2023 · FDA recall Z-1970-2023 · LumiraDx
Hazard
Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be more susceptible to breakage. If the swab breaks in the nasal cavity of a patient may cause injury or medical intervention to remove part of the swab · FDA Class II
Units
1003 kits
Sold at
US Nationwide distribution.
Description
Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be more susceptible to breakage. If the swab breaks in the nasal cavity of a patient may cause injury or medical intervention to remove part of the swab
Product
SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample collection in the intended nasal area. Catalog Number: 60566RevB
Manufacturer(s)
LumiraDx
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →