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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 4 of 10

Device	Model / Reference	Registries	Class	Status
Bluey	017276240467	FDA UDI	Class I	Active
Llama	017276237993	FDA UDI	Class I	Active
L.O.L. Surprise!	017276238785	FDA UDI	Class I	Unknown
Careband	017276237207	FDA UDI	Class I	Active
The Grinch	017276240801	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234107	FDA UDI	Class I	Active
Antibacterial PJ Masks Bandages	017276234633	FDA UDI	Class I	Unknown
Nerf	017276238013	FDA UDI	Class I	Active
CarePak	017276229127	FDA UDI	Class I	Active
CarePak	017276237900	FDA UDI	Class I	Active
SoundBody	481042886102	FDA UDI	N	Unknown
ALL-HEALTH Adhesive Bandages	017276233995	FDA UDI	Class I	Unknown
Care Science	00017276237559	FDA UDI	N	Active
CarePak	017276238136	FDA UDI	Class I	Active
Care Science	017276235463	FDA UDI	Class I	Active
Space Jam a new Legacy	017276237832	FDA UDI	Class I	Active
Sound Body	017276236736	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Cushions	017276233902	FDA UDI	Class I	Active
Emoji	017276238341	FDA UDI	Class I	Unknown
ALL-HEALTH Hydrocolloid Gel Bandages	017276233889	FDA UDI	Class I	Active
Clear Passage Nasal Strips	017276238549	FDA UDI	Class I	Active
Care Science	00017276236545	FDA UDI	N	Active
Crayola	017276237436	FDA UDI	Class I	Unknown
Summer	017276238747	FDA UDI	Class I	Unknown
CarePak	017276237948	FDA UDI	Class I	Active
Clear Passage	017276234800	FDA UDI	Class I	Active
Jurassic World	017276238716	FDA UDI	Class I	Unknown
Wonder Woman Antibacterial Bandages	017276236378	FDA UDI	Class I	Active
Care Science	017276238709	FDA UDI	Class I	Active
Care Science	017276235722	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Cushions	017276233940	FDA UDI	Class I	Unknown
Jurassic World	017276233209	FDA UDI	Class I	Unknown
Hershey's S'mores	017276237528	FDA UDI	Class I	Unknown
LOL Surprise Adhesive Bandages	017276237177	FDA UDI	Class I	Unknown
My Little Pony	017276237764	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276238846	FDA UDI	N	Unknown
CarePak	017276237924	FDA UDI	N	Active
ALL-HEALTH Adhesive Bandages	017276233988	FDA UDI	Class I	Unknown
Jojo Siwa Antibacterial Bandages	017276234879	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233766	FDA UDI	Class I	Unknown
Clear Passage	017276236910	FDA UDI	Class I	Active
minions	017276240825	FDA UDI	Class I	Active
Clear Passage Nasal Strips	017276234183	FDA UDI	Class I	Active
Batman	017276238358	FDA UDI	Class I	Active
CarePak	017276229448	FDA UDI	Class I	Active
Hershey	017276238730	FDA UDI	Class I	Unknown
ALL-HEALTH Adhesive Bandages	017276234145	FDA UDI	Class I	Active
CarePak	017276237887	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD2019	FDA UDI	Class I	Active
Sound Body	017276236583	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.