Aso Llc
300 SARASOTA CENTER BLVD., SARASOTA, FL, US
Registered product codes
26 product codes
Recent MDR events
638 on file
- TopCare healthJul 29, 2026Injury1038758-2026-00017
- ALL-HEALTHJun 4, 2026Injury1038758-2026-00013
- UP&UPJun 4, 2026Injury1038758-2026-00014
- CVS HEALTHMay 21, 2026Injury1038758-2026-00012
- EQUATE FIRST AID KITApr 29, 2026InjuryMW5187444
- EQUATE SMART HEAL HYDROCOLLOID GEL BANDAGESApr 2, 2026InjuryMW5186339
- ANTIBACTERIAL WATERPROOF ADHESIVE PADMar 25, 2026InjuryMW5185780
- EQUATEMar 18, 2026Injury1038758-2026-00008
- CVS HEALTHMar 18, 2026Injury1038758-2026-00009
- EQUATEMar 5, 2026Injury1038758-2026-00007
Recalls
15 on file
- Open, ClassifiedMay 2, 2023
The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the pad and is not disclosed on the labeling.
View FDA record ↗ - TerminatedAug 25, 2015
Contain 0.1% Benzalkonium Chloride in the 5/8 bandages inside the assortment which is not listed as an active ingredient in the product label.
View FDA record ↗ - TerminatedOct 1, 2013
No antibacterial bandages were packed in boxes labeled as antibacterial.
View FDA record ↗ - TerminatedAug 6, 2013
This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
View FDA record ↗ - TerminatedAug 6, 2013
This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
View FDA record ↗ - TerminatedAug 6, 2013
This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
View FDA record ↗ - TerminatedAug 6, 2013
This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
View FDA record ↗ - TerminatedAug 6, 2013
This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
View FDA record ↗ - TerminatedAug 6, 2013
This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
View FDA record ↗ - TerminatedAug 6, 2013
This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
View FDA record ↗
Compliance history
Matched by FEI 1038758.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.