CLASS III ONGOING Device recall · Reported 15 Mar 2023 · FDA Enforcement Report
Nobil Grip, product numbers 0102000 and 01202000-3 vials recalled
Preat is recalling Preat Nobil Grip, product numbers 0102000 and 01202000-3 vials, distributed nationwide in the US. The recall was initiated on 1 Feb 2023 and the FDA has classified it as Class III.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1226-2023
- FDA event ID
- 91614
- Recalling firm
- Preat, Santa Maria, CA
- Classification
- Class III
- Status
- Ongoing
- Recall initiated
- 1 Feb 2023
- FDA classified
- 6 Mar 2023
- Reported
- 15 Mar 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Device type
- Dental Devices
Timeline
| 1 Feb 2023 | Recall initiated by company | |
| 6 Mar 2023 | Classified by FDA | +33 days |
| 15 Mar 2023 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product is labeled with an incorrect expiration date.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.
Where it was distributed
Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, NC, NJ, NY, OK, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WV. There was also government distribution. The country of Canada.
Nationwide AlabamaArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMichiganMinnesotaMissouriMississippiNorth CarolinaNew Jersey
Questions about this recall
Is Nobil Grip, product numbers 0102000 and 01202000-3 vials recalled?
Yes. Preat recalled Nobil Grip, product numbers 0102000 and 01202000-3 vials on 1 Feb 2023. The recall is Class III and its status is Ongoing. Recall number Z-1226-2023.
Why was it recalled?
Product is labeled with an incorrect expiration date.
Which lots are affected?
Product #0102000 - Lot #21V0089; UDI 00842092127308. Product #0102000-3 - Lots 21V0089 and 194397; UDI 00842092155660.
Where was it sold?
Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, NC, NJ, NY, OK, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WV. There was also government distribution. The country of Canada.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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