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HomePRACTICON, INC. › Cool Cassette 2 Size 14 Instrument Tray Pure Purple

Cool Cassette 2 Size 14 Instrument Tray Pure Purple

PRACTICON, INC. · Model 7141913 PUR · UDI-DI 00723896008980

OFX
0
510(k) clearances
35
Adverse events
20
Recalls
42
Facilities

Description

Building on the success of the original Cool Cassette, the world’s first flexible silicone instrument trays, our Cool Cassette 2 Instrument Trays offer all the benefits of the original, with several design improvements to make your instrument-handling procedures easier and safer than ever!Like the original, Cool Cassette 2 is:Cooler—Solid silicone construction dissipates heat faster than steel for faster removal from the autoclave.Safer—No sharp edges to tear gloves or injure hands.Quieter—No metal to create noise, dull instruments, or scratch mirrors.Easier to open—Snap on lids "peel off" easily yet hold securely.More compact—Lids nest underneath, reducing space needed.Longer lasting—No hinges, locks, or moving parts to break.More colorful—Color-coded for operatory or instrument setups.Lighter—10% lighter weight than equivalent steel cassettes.Lower cost—About 40% less than equivalent steel cassettes.Based on feedback from users, the redesigned Cool Cassette 2 goes even further with the following improvements:Larger vent holes—For increased water and steam penetration.Wraparound perforations—For full drainage at any angle.Built-in lock buttons—Eliminate the need for safety bands.Longer—By 1/4" to accommodate ultrasonic scaler inserts.NEW size—In addition to the original three sizes, the new 10XL includes a 5-5⁄8" by 2-1⁄2"compartment for handpieces, syringes, or other items.NEW color—In addition to the original three colors, Cool Coral expands your color-coding options.Interior instrument saddles can be cut with scissors to accommodate large-handled instruments, if desired. All containers hold instruments up to 7-1⁄8" long. Available in 5, 10, 10XL, and 14 instrument sizes. Fully sterilizable to 375°F. Specify color.The Cool Cassette 2 14 Instrument Tray with two built-in A-W syringe tip clips measures 8-3⁄8"L x 8-3⁄8"W x 1-3⁄8"H outside.

Recalls

DateFirmReason
2026-05-04Medline Industries, LPDuring an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac
2026-03-19Medline Industries, LPDuring an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag
2025-03-03MEDLINE INDUSTRIES, LP - NorthfieldThere is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
2024-11-08Cardinal Health 200, LLCPotential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
2024-11-08Cardinal Health 200, LLCPotential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
2024-10-09MEDLINE INDUSTRIES, LP - NorthfieldMedline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
2024-09-04MEDLINE INDUSTRIES, LP - NorthfieldIt has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal
2024-06-27MEDLINE INDUSTRIES, LP - NorthfieldDue to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the pote

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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.