Home › ZIRC DENTAL PRODUCTS, INC. › E-Z Jett Cassette 10-Place Gray

E-Z Jett Cassette 10-Place Gray

ZIRC DENTAL PRODUCTS, INC. · Model 50Z930I · UDI-DI 00840161300522

FSM Prescription

510(k) clearances

2,231

Adverse events (2 deaths)

Recalls

874

Facilities

Description

"Holds 10 instruments Compartment in the middle to hold more instruments Open top, rounded holes and corners allow for superior water flow compared to normal cassettes Covers are attached to the cassette and open and fold back easily Dimensions: 7-15/16"" x 7"" x 1-1/8"" Contains Antimicrobial Protection Autoclavable up to 136°C/277F° Washer-disinfect"

Recalls

Date	Firm	Reason
2025-07-18	Encore Medical, LP	Their is a potential that the reamer may kick or bind up during or immediately prior to use.
2024-06-11	Medical Action Industries, Inc. 306	The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foa
2024-04-08	MEDLINE INDUSTRIES, LP - Northfield	Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma
2023-11-15	MEDLINE INDUSTRIES, LP - Northfield	Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile
2023-02-23	Aesculap Implant Systems LLC	Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct GTIN # is 04046955299607.
2022-12-15	Stradis Healthcare	Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.
2022-12-15	Stradis Healthcare	Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.
2021-11-24	Howmedica Osteonics Corp.	Triathlon Pro Tibial Preparation Tray may have been kitted with the Triathlon Cemented #1-3 Keel Punch (P/N: 6541-2-013) instead of the Triathlon Pro #0-3 Cemented Keel Punch (P/N:
2019-06-10	Zimmer Biomet, Inc.	Lack of an adequate sterilization validation.
2019-06-10	Zimmer Biomet, Inc.	Lack of an adequate sterilization validation.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.