Device recalls

ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthetic restorations such…

Hiossen Inc. · Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini versio…

Open, ClassifiedUnder Investigation by firmZ-1275-2025
Open FDA's page for this record
Cfres ID
212258
Product res number
Z-1275-2025
Event date initiated
2025-01-27
Event date posted
2025-03-05
Recall status
Open, Classified
Res event number
96178
Product code
NHA
Code info
Lot Code: UDI-DI: 00814913026312 Lot# H4E21G062
Firm FEI number
3007135442
Recalling firm
Hiossen Inc.
Address 1
85 Ben Fairless Dr
City
Fairless Hills
State
PA
Postal code
19030-5012
Additional info contact
Mateusz Leszczak 201-2660657
Root cause description
Under Investigation by firm
Product quantity
19 units
Distribution pattern
US Nationwide distribution.
Product description

ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4524MP

Reason for recall

Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version

Action

Hoissen issued URGENT: MEDICAL DEVICE RECALL-CORRECTION letter on 1/27/25 via USPS Certified Mail. Letter states reason for recall, health risk and action to take. Immediate Actions to be taken by You, the clinician: 1. Do not use the affected devices 2. Quarantine (separate) the affected devices in a different location, away from normal stock room. 3.Immediately fill out the Acknowledgement and Receipt Form* (Fax: 267-795-7031 or Email: recall@hiossen.com ) *Response is required regardless if the devices have already been return or implanted 4. Return quarantined devices to the following address or contact your sales representative for assistance. ATTN: Peter Lee / Recall 85 Ben Fairless Dr. Fairless Hills, PA 19030 5. Replacement patient chart stickers will be provided so that you may include the corrected chart sticker in the patient s medical records as applicable. Hiossen has already deployed a permanent corrective action to address the issue described in this Recall Notice. Hiossen investigated and identified the source of the issue and has already implemented new procedures which eliminates the potential for further mis-labeling. Other Information If you need any further information or support concerning this recall/issue, please reach HIOSSEN: Monday through Friday, 8:00 AM to 4:30 PM, Eastern Time. Tel: 267-795-7031 Email: recall@hiossen

K numbers
K130662
Harmonized identifiers (openFDA)
Device name
Abutment, Implant, Dental, Endosseous
Medical specialty description
Dental
Regulation number
872.3630
Device class
2
K number
K223395, K203456, K140600, K063403, K183518, K221972, K223496, K240725, K961728, K190040, K182091, K053099, K073345, K052823, K213961, K253999, K063106, K160382, K060880, K101068, K083474, K170356, K080239, K083324, K081666, K093780, K150899, K971706, K262207, K083871, K071551, K023631, K122988, K073217, K073553, K121843, K091701, K163350, K121709, K102467 +676 more
Registration number
1226544, 3023265483, 9613866, 3006973441, 3007362683, 3005730680, 3011587630, 1038806, 1424785, 3012635238, 3010860907, 2244842, 9613283, 3005031178, 3007283751, 3011808221, 3023535580, 3012187973, 3036779616, 3004417597, 3031162123, 8031058, 3030690317, 3009756327, 3007597023, 1036836, 3008088588, 3007135442, 3009727738, 3018077122, 3005554774, 3003402534, 3013465593, 2133778, 2530808, 3005503242, 3011649314, 3010303805, 3017450159, 3009514134 +342 more
FEI number
3023265483, 3006973441, 3007362683, 3005730680, 3011587630, 1038806, 3012635238, 3010860907, 2244842, 3005031178, 3007283751, 3011808221, 3023535580, 3012187973, 3036779616, 3004417597, 3031162123, 3030690317, 3007597023, 1036836, 3008088588, 3007135442, 3009727738, 3018077122, 3005554774, 3002768455, 3003402534, 3013465593, 3005503242, 1000272060, 3011649314, 3010303805, 3017450159, 3009514134, 3003394627, 3005597557, 3012205930, 3039641923, 3003024548, 3002807050 +342 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.