Preat Corp Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
Brand
Preat Corp
Lot Codes / Batch Numbers
UDI-DI: 00842092161364/Lot # OF018356
Products Sold
UDI-DI: 00842092161364/Lot # OF018356
Preat Corp is recalling Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental due to The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
Recommended Action
Per FDA guidance
On August 4, 2023, Preat Corporation issued a "Urgent Medical Device Recall" notification via: USPS. Preat ask consignees to take the following actions: Product within the scope of the recall shall be discarded or returned to Preat Corporation. Instructions for the return will be provided. Complete and email response form to Nichole Fetterman, E-Mail: nfetterman@younginnovations.com or mail to Preat Corporation, Attn. Nichole Fetterman, 2625 Skyway Drive, Ste. B, Santa Maria, CA 93455
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, NJ, OH, OR, SC, TX
Page updated: Jan 10, 2026