Drugs & medicalClass II

Biomet, Inc. recalls BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair

There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop

Read the official notice →
Date
2025-10-29
Country
United States
Brand
Biomet
Product
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
Classification
Class II
Units
Refer to the attached ZFA 2025-00166_Initial Consignee List and ZFA…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Biomet recalls

  1. 2026-08-12
  2. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mm

    Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

    FDA · DeviceBiomet, Inc.Refer to the attached ZFA 2026-00096_Initial Consignee List and ZFA…Official notice →
  3. 2025-10-01
  4. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

    The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.

    FDA · DeviceBiomet, Inc.US Nationwide distribution.Official notice →
  5. 2024-11-27
  6. US
    Drugs & medicalClass II

    Biomet, Inc. recalls JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357

    Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to…

    FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide and the countries of Australia, Brazil,…Official notice →
  7. 2024-07-03
  8. US
    Drugs & medicalClass II

    Biomet, Inc. recalls RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206

    41 mm acetabular outer heads were potentially assembled with a 42 mm locking ring, may lead to joint instability leading requiring surgical intervention

    FDA · DeviceBiomet, Inc.Worldwide - US Nationwide distribution in the states of AZ, CA, NJ, PA, TX, VA…Official notice →
  9. 2024-05-01
  10. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a foil pouch with…

    Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.

    FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide in the state of IN and the countries of…Official notice →
  11. 2023-12-27
  12. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Biolox Ceramic Option Head Zimmer 12/14 40mm +0, Item Number 00-8777-040-02

    One product complaint was received reporting that there was an incorrect adapter in the packaging. An adapter with neck length M/+0 was inside the product packaging, which should have contained an adapter with neck…

    FDA · DeviceBiomet, Inc.US States: AL, CA, MD, MI, NC, OH, OK, TN, TX. Netherlands.Official notice →
All 14 Biomet recalls →

Other drugs & medical recalls in the United States

  1. 2025-10-29
  2. US
    Drugs & medicalClass II

    UIH Technologies LLC recalls Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT ATLAS MD, Rx Only

    Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

    FDA · DeviceUIH Technologies LLCUS: OUS:Official notice →
  3. US
    Drugs & medicalClass II

    Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer, Part Number C11137

    Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering…

    FDA · DeviceBeckman Coulter, Inc.Worldwide - US Nationwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    Wipro GE Healthcare Private Ltd. recalls GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03; Medical…

    Carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs…

    FDA · DeviceWipro GE Healthcare Private Ltd.Worldwide distribution.Official notice →
  5. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3…

    Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

    FDA · DeviceCardinal Health 200, LLCWorldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →
  6. US
    Drugs & medicalClass I

    ICU Medical, Inc. recalls IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set…

    IV Gravity burette administration set burette component is missing an internal shutoff valve intended to stop fluid flow, which if used may result in delay in therapy during setup, over delivery/unrestricted flow, or…

    FDA · DeviceICU Medical, Inc.Worldwide distribution: US (nationwide) to states of: TX, SC and OUS (foreign)…Official notice →
  7. US
    Drugs & medicalClass I

    Abiomed, Inc. recalls Automated Impella Controller (AIC) labeled as the following with corresponding Product Codes: 1. AIC w/Impella Connect for ECP, Product…

    Potential for Automated Impella Controller (AIC) purge pressure issues due to purge retainer failures.

    FDA · DeviceAbiomed, Inc.Worldwide distribution. US Nationwide, Australia, Austria, Belgium, Brazil,…Official notice →
See all drugs & medical recalls →