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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 8 of 10

Device	Model / Reference	Registries	Class	Status
Build A Bear	017276238488	FDA UDI	Class I	Active
Care Science	017276234695	FDA UDI	U	Active
Care Science	00017276237368	FDA UDI	N	Active
Care Science	017276234770	FDA UDI	Class I	Active
Ryans World	017276237443	FDA UDI	Class I	Unknown
Care Science	017276238983	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233742	FDA UDI	Class I	Unknown
Nerf	017276238723	FDA UDI	Class I	Active
Advanced Wart Freeze	017276237313	FDA UDI	Class II	Unknown
Care Band	CBD6418	FDA UDI	Class I	Active
Jurassic World	017276233117	FDA UDI	Class I	Active
LOL Surprise Antibacterial Bandages	017276235302	FDA UDI	Class I	Unknown
My Martin's	041520091017	FDA UDI	Class I	Unknown
SoundBody	017276237733	FDA UDI	N	Unknown
Crayola First Aid Kit	017276240054	FDA UDI	N	Active
Care Science	017276238952	FDA UDI	U	Active
Clear Passage Nasal Strips	017276238617	FDA UDI	Class I	Active
Sound Body	017276237726	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233667	FDA UDI	Class I	Active
Rudolph	017276235616	FDA UDI	Class I	Active
InstaClear	017276233780	FDA UDI	Class I	Unknown
SpongeBob Square pants	017276233551	FDA UDI	Class I	Active
Bluey	017276240856	FDA UDI	Class I	Active
Care Science	00017276236101	FDA UDI	N	Active
ALL-HEALTH Adhesive Bandages	017276234114	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233681	FDA UDI	Class I	Unknown
ALL-HEALTH Adhesive Bandages	017276234084	FDA UDI	Class I	Active
CarePak	017276238099	FDA UDI	Class I	Unknown
Scoob Antibacterial Bandages	017276236934	FDA UDI	Class I	Active
L.O.L. Surprise!	017276238020	FDA UDI	Class I	Unknown
Care Science	017276236804	FDA UDI	Class I	Active
Afro Unicorn	017276239126	FDA UDI	Class I	Active
Sesame Street	017276237450	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD2022	FDA UDI	Class I	Active
Sound Body	017276236743	FDA UDI	Class I	Active
Rainbow Magic	017276238570	FDA UDI	Class I	Unknown
Sound Body	017276236767	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234039	FDA UDI	Class I	Unknown
ALL-HEALTH Hydrocolloid Gel Cushions	017276233926	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234428	FDA UDI	Class I	Active
Sound Body	017276236484	FDA UDI	Class I	Active
Yummy Animal	017276238006	FDA UDI	Class I	Active
The Elf on the Shelf	017276238440	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Bandages	017276233834	FDA UDI	Class I	Active
Space Jam a new legacy	017276237511	FDA UDI	Class I	Unknown
Neon Crayola	017276240443	FDA UDI	Class I	Active
Rapid Seal	00017276239393	FDA UDI	N	Active
Care Science	017276235265	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234459	FDA UDI	Class I	Active
Wonder Woman Antibacterial Bandages	017276236781	FDA UDI	Class I	Unknown

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.