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Aso LLC

United States·US-MF-000008641

Last updated September 17, 2026

Information

Country: United States
Address: 300, Sarasota Center Blvd., Sarasota, United States
Website: www.asoeurope.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +31 24 343 54 80
PRRC Contact: Federico Juliao
EUDAMED SRN: US-MF-000008641
FDA FEI Number: 1038758
DUNS Number: 152793493

Catalogue (478)

Page 6 of 10

Device	Model / Reference	Registries	Class	Status
ALL-HEALTH Adhesive Bandages	017276234053	FDA UDI	Class I	Unknown
Emoji	017276230734	FDA UDI	Class I	Active
CarePak	017276238303	FDA UDI	Class I	Active
Jurassic World	017276237412	FDA UDI	Class I	Unknown
Advanced Wart Freeze	017276237320	FDA UDI	Class II	Unknown
Care Science	017276235241	FDA UDI	Class I	Unknown
Care Science	017276238525	FDA UDI	Class I	Active
Rapid Seal	017276239416	FDA UDI	U	Active
Nerf	017276236460	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Bandages	017276233858	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234015	FDA UDI	Class I	Unknown
Clear Passage Nasal Strips	017276238631	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234046	FDA UDI	Class I	Unknown
ALL-HEALTH Hydrocolloid Gel Bandages	017276234152	FDA UDI	Class I	Active
Care Science	017276238495	FDA UDI	Class I	Active
Sound Body	017276228434	FDA UDI	Class I	Unknown
Ryans World Adhesive Bandages	017276237184	FDA UDI	Class I	Unknown
CarePak	017276238334	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233674	FDA UDI	Class I	Unknown
Gabby's Dollhouse	017276239133	FDA UDI	Class I	Active
Clear Passage Nasal Strips	017276232998	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234022	FDA UDI	Class I	Unknown
minions	017276240726	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233735	FDA UDI	Class I	Unknown
Sound Body	017276236750	FDA UDI	Class I	Active
Care Science	017276235395	FDA UDI	Class I	Active
Bluey	017276239720	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233704	FDA UDI	Class I	Unknown
ALL-HEALTH Adhesive Bandages	017276234008	FDA UDI	Class I	Unknown
Children's Miracle Network Hospitals	017276235180	FDA UDI	Class I	Unknown
Rapid Seal	00017276237382	FDA UDI	U	Active
The Cat In The Hat	017276240795	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234480	FDA UDI	Class I	Active
Care Science	017276235715	FDA UDI	Class I	Active
Care Science	017276234701	FDA UDI	Class I	Unknown
Rapid Seal	017276240160	FDA UDI	U	Active
Jurassic World	017276238839	FDA UDI	Class I	Unknown
Candy Land	017276237962	FDA UDI	Class I	Unknown
Antibacterial PJ Masks Bandages	017276232820	FDA UDI	Class I	Active
L.O.L. surprise!	017276236439	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234077	FDA UDI	Class I	Active
Bluey	017276239300	FDA UDI	Class I	Active
Crayola	017276239669	FDA UDI	Class I	Active
LOL Surprise Adhesive Bandages	017276235579	FDA UDI	Class I	Unknown
CarePak	017276230598	FDA UDI	N	Active
Care Science	017276239683	FDA UDI	Class I	Active
JOJO Siwa	017276235562	FDA UDI	Class I	Active
CarePak	017276228939	FDA UDI	N	Unknown
Crayola	017276237801	FDA UDI	N	Active
Barbie	017276239904	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

Aso Europe BV NL

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (15)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Mar 23, 2023	Z-1499-2023	—	open, classified	The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the pad and is not disclosed on the labeling.
Jun 22, 2022	Z-1517-2022	—	open, classified	The product falls apart during handling after removal from its primary packaging.
Mar 2, 2022	Z-1031-2022	—	terminated	Kits contained recalled acetaminophen.
Oct 16, 2018	Z-0525-2019	—	open, classified	Potential that gauze pads may not be fully sterilized
Jun 10, 2015	Z-2460-2015	—	terminated	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.
Aug 21, 2013	Z-0004-2014	—	terminated	No antibacterial bandages were packed in boxes labeled as antibacterial.
Jul 26, 2013	Z-1890-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1892-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1891-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1894-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1893-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1895-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1896-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1889-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1888-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.