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.
Read the official notice →- Date
- 2023-11-15
- Country
- United States
- Brand
- Young Dental Manufacturing I
- Product
- CONTRA GRAY (soft) TURBO PLUS CUPS, REF 153112. Dental Prophylaxis Angles
- Classification
- Class II
- Units
- US: IN, TN, MO
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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
- 2024-10-09
USYoung 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 →- 2024-06-19
- US
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 → - 2023-06-14
- US
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 → - 2022-12-28
- US
Young Dental Manufacturing I, LLC recalls Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
mislabeled product
FDA · DeviceYoung Dental Manufacturing I, LLCWorldwide distribution - US Nationwide distribution in the states of IA, NY,…Official notice →
Other drugs & medical recalls in the United States
- 2023-11-15
- US
Olympus Corporation of the Americas recalls EVIS EXERA III Gastrointestinal Videoscope
Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel.
- US
- US
Cordis US Corp recalls Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
Non-sterile product labeled as sterile was distributed.
- US
Philips Ultrasound, Inc. recalls Philips Affiniti 70, Diagnostic Ultrasound System Model # 795210
Their is the potential that diagnostic ultrasound systems operating with software version 10.0 may present a delayed image instead of a real time image.
FDA · DevicePhilips Ultrasound, Inc.US: AZ, CA, CT, FL, GA, ID, IL, KY, MD, MT, NE, NV, OH, TN, TX, UT, VA OUS:…Official notice → - US
Encore Medical, LP recalls RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, orthopedic shoulder implant component.
Two different humeral socket Insert devices were swapped during packaging, which could result in surgeons not having the correct device for surgery, which could cause a delay in surgery.
FDA · DeviceEncore Medical, LPUS: MN, TX, IN, OH, SC, RI, ME, NJ, NY, KS, LA, FL, CAOfficial notice → - US
Philips North America Llc recalls DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.
Potential for units suspended on the ceiling to fail and fall.