Drugs & medicalClass III

Young Dental Manufacturing I, LLC recalls Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714

mislabeled product

Read the official notice →
Date
2022-12-28
Country
United States
Brand
Young Dental Manufacturing I
Product
Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
Classification
Class III
Units
Worldwide distribution - US Nationwide distribution in the states of IA, NY,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Young Dental Manufacturing I recalls

  1. 2024-10-09
  2. US
    Drugs & medicalClass II

    Young Dental Manufacturing I, LLC recalls BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of solution.

    The bulk product used in the recalling firm's repackaged finished product was recalled due to bacterial contamination.

    FDA · DeviceYoung Dental Manufacturing I, LLCDistribution was made to AZ, ID, MD, NV, NY, PA, SC, TN, TX, WI. There was no…Official notice →
  3. 2024-06-19
  4. US
    Drugs & medicalClass II

    Young Dental Manufacturing I, LLC recalls Darby Prophylaxis Paste with 1.23% Fluoride Ion, Mint Coarse

    Part number 040032, Lot number, 248607 was incorrectly labeled as part number 045032

    FDA · DeviceYoung Dental Manufacturing I, LLCUS Nationwide distribution in the state of TN.Official notice →
  5. 2023-11-15
  6. US
    Drugs & medicalClass II

    Young Dental Manufacturing I, LLC recalls CONTRA GRAY (soft) TURBO PLUS CUPS, REF 153112. Dental Prophylaxis Angles

    one lot of Contra Gray (soft) Turbo Plus Cups Dental Prophylaxis Angles may contain Contra Petite Web LF Soft Purple Cup DPAs.

    FDA · DeviceYoung Dental Manufacturing I, LLCUS: IN, TN, MOOfficial notice →
  7. 2023-06-14
  8. US
    Drugs & medicalClass II

    Young Dental Manufacturing I, LLC recalls BencoDental iris 5% NaF varnish, WHITE MINT ITEM # 4323-635; cavity varnish

    The Iris 5% Fluoride Varnish White Mint package lot 207540 may contain units of 5% Fluoride Varnish Bubblegum.

    FDA · DeviceYoung Dental Manufacturing I, LLCUS distribution to Florida, Nevada, and Pennsylvania.Official notice →
All 5 Young Dental Manufacturing I recalls →

Other drugs & medical recalls in the United States

  1. 2022-12-28
  2. US
    Drugs & medicalClass II

    GE Medical Systems, LLC recalls B105P Patient Monitor (with E-module slot option), REF 6160000-001-XXXXXX,

    GE Healthcare has become aware that if certain B1x5P / B1x5M patient monitors use "mmHg" or "kPa" as the unit for CO2 measurement, the displayed value for CO2 measurement can be inaccurate when used in a location that…

    FDA · DeviceGE Medical Systems, LLCWorldwide distribution.Official notice →
  3. US
    Drugs & medicalClass II

    Icotec Ag recalls VADER Pedicle System Torque Wrench, Hudson Coupling, 12 Nm, REF 42-702

    During internal testing (at manufacturer site) of two torque wrench devices, it was detected that the torque limiting function was out of specification. The specified torque limiting value is 12 Nm. The measuring…

    FDA · DeviceIcotec AgUS Nationwide distribution in the state of GA.Official notice →
  4. US
    Drugs & medicalClass II

    Corin Ltd recalls Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615

    The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.

    FDA · DeviceCorin LtdUS Nationwide distribution in the states of FL, GA, MA, MI, Ok, PA, TX.Official notice →
  5. US
    Drugs & medicalClass II

    DeVilbiss Healthcare LLC recalls DeVilbiss, 525 5-liter Oxygen Concentrator Models 525DS, 525DS-Q

    The firm has received complaints of the device becoming hot. The firm has updated the user manual to include warnings that applied parts in contact with the patient may in some situations exceed 41 degrees Celsius…

    FDA · DeviceDeVilbiss Healthcare LLCUS Nationwide. Foreign distribution pending.Official notice →
  6. US
    Drugs & medicalClass II

    ConvaTec, Inc recalls ConvaTec AQUACEL Foam Ag Adhesive, wound dressing advesive

    ConvaTec are voluntarily recalling a batch of AQUACEL¿ Foam Ag Adhesive 10cm x 10cm (x 10 pack) due to the identification of visual contamination in the form of brown spots present on several dressings.

    FDA · DeviceConvaTec, IncUS Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    GE Medical Systems, LLC recalls Centricity Universal Viewer 6.0. Used to display medical images (Including mammograms) and data from various imaging sources.

    There is the potential that after installation of the IAS tool, some studies can remain hidden without user notification. Access to those hidden studies requires GE Healthcare assistance, which can result in a delay in…

    FDA · DeviceGE Medical Systems, LLCNationwide distribution to CA, CO, DE, FL, IA, IL, MA, MI, MN, MO, MS, MT, ND,…Official notice →
See all drugs & medical recalls →