Recall Z-0957-2019— Cardinal Health 200, LLC
Class II · Terminated
Class II FDA medical device recall by Cardinal Health 200, LLC, initiated 2018-12-27, terminated 2020-06-29. FDA's recall record names no specific 510(k) clearance for this event. Product: Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm) Product Code: 8044 - Product Usage: Ideal for applying ointments, prepping, wiping needles, cleaning slides and more Rayon/polyester blend construction Highly absorbent.. Reason: Curity All Purpose Sponges were not sterilized and distributed.
- Recalling firm
- Cardinal Health 200, LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-12-27
- Terminated
- 2020-06-29
- Firm location
- Mansfield, MA, United States
Product description
Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm) Product Code: 8044 - Product Usage: Ideal for applying ointments, prepping, wiping needles, cleaning slides and more Rayon/polyester blend construction Highly absorbent.
Reason for recall
Curity All Purpose Sponges were not sterilized and distributed
Data sourced from openFDA. This site is unofficial and independent of the FDA.