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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 3 of 10

Device	Model / Reference	Registries	Class	Status
Clear Passage	017276236927	FDA UDI	Class I	Active
Jurassic World	017276238754	FDA UDI	Class I	Active
Clear Passage	017276234817	FDA UDI	Class I	Unknown
CarePak	017276229066	FDA UDI	Class I	Active
Peeps	017276238563	FDA UDI	Class I	Unknown
Care Science	017276234688	FDA UDI	U	Active
InstaClear	017276233797	FDA UDI	Class I	Active
CarePak	017276237641	FDA UDI	Class I	Active
Sesame Street	017276233391	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233759	FDA UDI	Class I	Unknown
ALL-HEALTH Adhesive Bandages	017276233711	FDA UDI	Class I	Unknown
Hot Wheels	017276239980	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234060	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234435	FDA UDI	Class I	Active
yummy animal	017276237269	FDA UDI	Class I	Unknown
Care Science	017276234671	FDA UDI	U	Active
Sound Body	481042591105	FDA UDI	Class I	Unknown
Care Science	00017276237771	FDA UDI	N	Active
My Little Pony	017276237566	FDA UDI	Class I	Unknown
Care Science	017276240337	FDA UDI	Class I	Active
minions	017276240054	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD2027	FDA UDI	Class I	Active
Sesame Street	017276240450	FDA UDI	Class I	Active
Care Science	017276238938	FDA UDI	Class I	Active
Rudolph the red-nosed reindeer	017276235760	FDA UDI	Class I	Active
Nickelodeon Sponge Bob Square Pants	017276234572	FDA UDI	Class I	Unknown
The Grinch	017276240863	FDA UDI	Class I	Active
Care Science	017276238969	FDA UDI	U	Active
Care Science	017276237375	FDA UDI	Class I	Active
CarePak	017276238082	FDA UDI	Class I	Active
Barbie	017276239973	FDA UDI	Class I	Active
Care Science	017276239287	FDA UDI	Class I	Active
CarePak	017276238068	FDA UDI	Class I	Active
Sesame Street	017276237467	FDA UDI	Class I	Active
Sound Body	017276236576	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Cushions	017276233933	FDA UDI	Class I	Active
JOJO Siwa	017276237757	FDA UDI	Class I	Active
Little Monsters	017276238815	FDA UDI	Class I	Active
Frosty the snowman	017276238426	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD4018	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234442	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Bandages	017276233865	FDA UDI	Class I	Active
Care Science	017276240344	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD1018	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Bandages	017276234169	FDA UDI	Class I	Active
Careband	017276237221	FDA UDI	Class I	Active
Easy Breathe	850000495234	FDA UDI	Class I	Unknown
Garfield	017276221169	FDA UDI	Class I	Active
Batman	017276238273	FDA UDI	Class I	Active
Care Science	017276237610	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.