Is this your brand? Sign in to claim ownership.

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 7 of 10

Device	Model / Reference	Registries	Class	Status
Care Science	017276234794	FDA UDI	Class II	Active
Emoji	017276238044	FDA UDI	Class I	Active
CarePak	017276237665	FDA UDI	Class I	Active
Elf	017276238440	FDA UDI	Class I	Active
Scoob! Adhesive Bandages	017276236835	FDA UDI	Class I	Active
CarePak	017276237603	FDA UDI	Class I	Active
CarePak	017276238051	FDA UDI	Class I	Active
Clear Passage Nasal Strips	017276238594	FDA UDI	Class I	Active
Dreamworks Spirit Untamed	017276237405	FDA UDI	Class I	Unknown
Candy Land	017276236903	FDA UDI	Class I	Unknown
CarePak	017276229110	FDA UDI	Class I	Active
The Elf on the Shelf	017276238891	FDA UDI	Class I	Unknown
Care Science	017276237498	FDA UDI	Class I	Active
Care Science	017276234732	FDA UDI	Class I	Unknown
Latter-Day Armor Adhesive Bandages	860001904314	FDA UDI	Class I	Unknown
Crayola	017276240030	FDA UDI	Class I	Active
CarePak	017276237870	FDA UDI	Class I	Active
Care Science	017276235272	FDA UDI	Class I	Active
CarePak	017276237672	FDA UDI	Class I	Unknown
Care Science	B07CGFT1FF	FDA UDI	N	Unknown
Garfield	017276980233	FDA UDI	Class I	Unknown
Clear Passage Nasal Strips	017276232967	FDA UDI	Class I	Active
Peeps	017276237276	FDA UDI	Class I	Unknown
Clear Passage Nasal Strips	017276232981	FDA UDI	Class I	Active
Miraculous	017276239126	FDA UDI	Class I	Active
Crayola	017276970456	FDA UDI	Class I	Active
Ryan's World	017276237054	FDA UDI	Class I	Unknown
CarePak	017276237627	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234473	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD1321	FDA UDI	Class I	Active
CarePak	017276238297	FDA UDI	Class I	Active
Sonic The Hedgehog	017276239096	FDA UDI	Class I	Unknown
Sound Body	017276236590	FDA UDI	Class I	Unknown
Bluey	017276239409	FDA UDI	Class I	Active
CarePak	017276237917	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Bandages	017276233896	FDA UDI	Class I	Active
Care Science	017276234787	FDA UDI	Class I	Active
CarePak	017276229134	FDA UDI	Class I	Active
Sesame Street The Nutcracker	0172762397130	FDA UDI	Class I	Active
Celebrate with Reese's	017276238822	FDA UDI	Class I	Active
ALL-HEALTH Performance Series	017276234503	FDA UDI	Class I	Unknown
Emoji	017276230703	FDA UDI	Class I	Active
Ryan's World	017276236897	FDA UDI	Class I	Unknown
PJ Masks	017276238037	FDA UDI	Class I	Active
Jurassic World Dominion	017276238778	FDA UDI	Class I	Unknown
Careband	017276237214	FDA UDI	Class I	Active
CarePak	017276229097	FDA UDI	Class I	Active
Care Science	017276237542	FDA UDI	N	Active
Care Science	017276235258	FDA UDI	Class I	Unknown
Careband- EMOJI	184256	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.