Recall Atlas
Drugs & medicalClass II

Howmedica Osteonics Corp. recalls TS Universal Baseplate Finishing Tray, Triathlon. Catalog Number: 6543-6-506.

Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual…

Read the official notice →
Date
2026-10-21
Country
United States
Brand
Howmedica Osteonics
Product
TS Universal Baseplate Finishing Tray, Triathlon. Catalog Number: 6543-6-506.
Classification
Class II
Units
These trays are provided by sale or loan. Loans are provided through…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Howmedica Osteonics recalls

  1. 2026-09-23
  2. Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components…

    Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in…

    FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide and the countries of Canada, LATAM,…Official notice →
  3. 2026-06-24
  4. Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.

    Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot…

    FDA · DeviceHowmedica Osteonics Corp.US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.Official notice →
  5. 2026-03-25
  6. Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

    A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and…

    FDA · DeviceHowmedica Osteonics Corp.Domestic: Nationwide Distribution; International: Australia, Germany, Belgium,…Official notice →
  7. 2025-12-31
  8. Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR)…

    When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.

    FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide and the countries of Canada, Germany,…Official notice →
  9. 2025-10-08
  10. Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls 1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0580-1-352;

    a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.

    FDA · DeviceHowmedica Osteonics Corp.International distribution in the country of United Kingdom.Official notice →
  11. 2024-10-16
  12. Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls MAKO Integrated Cutting System (MICS) HANDPIECE, Catalog Number 209063

    Stryker has identified an issue with the characterization process that impacted the constant values assigned to the associated MICS Handpieces.

    FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide and the countries of Australia, Germany.Official notice →
All 29 Howmedica Osteonics recalls →

Other drugs & medical recalls in the United States

  1. 2026-10-21
  2. Drugs & medicalClass II

    INTELERAD MEDICAL SYSTEMS INCORPORATED recalls IntelePACS, InteleConnect Portal/Tech Portal Versions PACS-5-1-1-R102, PACS-5-2-1-R93, PACS-5-3-1-R83 through R128,…

    Following a Chromium-based web-browser, report and displayed images may not match.

    FDA · DeviceINTELERAD MEDICAL SYSTEMS INCORPORATEDUS Nationwide distribution.Official notice →
  3. Drugs & medicalClass II

    Medline Industries, LP recalls Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M

    Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.Official notice →
  4. Drugs & medicalClass II

    Medline Industries, LP recalls Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L; 2) OPEN HEART ACCESSORY…

    Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution.Official notice →
  5. Drugs & medicalClass II

    Cook Incorporated recalls Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder wall, Reference Part…

    The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing. Potential events that may occur as a result of…

    FDA · DeviceCook IncorporatedUS States: FL, IL, NM, TX, WA. Canada, France, Germany, Italy, Spain,…Official notice →
  6. Drugs & medicalClass III

    Magellan Diagnostics, Inc. recalls LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.

    In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct expiration date is July 13, 2026. If used the system will display…

    FDA · DeviceMagellan Diagnostics, Inc.US Nationwide distribution in the states of CA, IN, PA, TX, NE, IL, MA, MO, KY.Official notice →
  7. Drugs & medicalClass II

    Beckman Coulter, Inc. recalls DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513

    The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check valve replacement was excluded from the annual…

    FDA · DeviceBeckman Coulter, Inc.Worldwide - US Nationwide distribution including in the states and territory…Official notice →
See all drugs & medical recalls →