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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 5 of 10

Device	Model / Reference	Registries	Class	Status
Care Science	017276238532	FDA UDI	Class I	Active
Td	017276238990	FDA UDI	Class I	Active
Crayola	017276237115	FDA UDI	Class I	Active
Care Science	00017276236699	FDA UDI	Class I	Unknown
Elf	017276238907	FDA UDI	Class I	Unknown
Care Band Adhesive Bandages	CBD4025	FDA UDI	Class I	Active
Care Science	017276238624	FDA UDI	Class I	Active
CarePak	017276238310	FDA UDI	Class I	Active
Ryan's World	017276237108	FDA UDI	Class I	Unknown
CarePak	017276237689	FDA UDI	Class I	Unknown
Care Science	017276236798	FDA UDI	Class I	Active
Sparkle & Shine Antibacterial Bandages	017276240498	FDA UDI	Class I	Active
CarePak	017276237931	FDA UDI	Class I	Active
InstaClear	017276233827	FDA UDI	Class I	Active
Sound Body	017276236477	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD5118	FDA UDI	Class I	Active
Sound Body	017276229707	FDA UDI	Class I	Unknown
Care Science	017276234749	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233971	FDA UDI	Class I	Unknown
CarePak	017276229141	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Bandages	017276233841	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD2760	FDA UDI	Class I	Active
Rapid Seal	00017276237399	FDA UDI	U	Active
Sound Body	017276236606	FDA UDI	Class I	Unknown
CarePak	017276238327	FDA UDI	Class I	Active
Bluey	017276240818	FDA UDI	Class I	Active
Jurassic World Camp Cretaceous	017276238693	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276233698	FDA UDI	Class I	Unknown
Care Science	017276235401	FDA UDI	Class I	Active
InstaClear	017276233810	FDA UDI	Class I	Active
Peeps	017276239812	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234091	FDA UDI	Class I	Unknown
ALL-HEALTH Adhesive Bandages	017276233964	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234497	FDA UDI	Class I	Active
Crayola	017276237337	FDA UDI	Class I	Active
All-Health	B07D1CVLV3	FDA UDI	Class II	Unknown
Sound Body	017276236613	FDA UDI	Class I	Active
Care Science	017276237481	FDA UDI	Class I	Active
CarePak	017276229073	FDA UDI	Class I	Active
Bubble Guppies	017276237573	FDA UDI	Class I	Unknown
Care Science	017276235227	FDA UDI	Class I	Unknown
Sound Body	017276229714	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD4022	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD1019	FDA UDI	Class I	Active
SpongeBob Square pants	017276237597	FDA UDI	Class I	Active
Bluey	017276240993	FDA UDI	Class I	Active
Hasbro Gaming	017276237429	FDA UDI	Class I	Unknown
SpongeBob Squarepants	017276237580	FDA UDI	Class I	Unknown
CarePak	017276237634	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Cushions	017276233919	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.