Drugs & medicalClass II

Zimmer, Inc. recalls Z1 Femoral Hip System, Product Number 611777612

There is a potential design issue with the Z1 Offset Stem Inserter leading to fracturing of the distal tip.

Read the official notice →
Date
2025-03-19
Country
United States
Brand
Zimmer
Product
Z1 Femoral Hip System, Product Number 611777612
Classification
Class II
Units
US Nationwide distribution.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Zimmer recalls

  1. 2025-11-12
  2. US
    Drugs & medicalClass II

    Zimmer, Inc. recalls Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing, Model/Catalog Number:…

    Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E¿ Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package…

    FDA · DeviceZimmer, Inc.US: OH, GA, WI, NE, IA, IL, CA, NY, MD, NC, PA, AL, TN, MI, WA, FL, TX, KS,…Official notice →
  3. 2025-04-30
  4. US
    Drugs & medicalClass II

    Zimmer, Inc. recalls Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained,…

    The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stainless-steel femoral stems.

    FDA · DeviceZimmer, Inc.Worldwide distribution - US Nationwide and the countries of Panama, Hong Kong,…Official notice →
  5. 2025-04-02
  6. US
    Drugs & medicalClass II

    Zimmer, Inc. recalls NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model Number 00-5962-042-10

    The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label does not match with the compatibility statements "USE WITH PLATE 5, 6" in the translations section of the same label.

    FDA · DeviceZimmer, Inc.Worldwide - US Nationwide distribution in the states pf CA, KS, MA, MD, ME,…Official notice →
  7. 2025-02-05
  8. US
    Drugs & medicalClass II

    Zimmer, Inc. recalls NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10

    It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.

    FDA · DeviceZimmer, Inc.Worldwide - US Nationwide distribution in the states of CA, FL, GA, KS, MO,…Official notice →
  9. 2024-11-13
  10. US
    Drugs & medicalClass II

    Zimmer, Inc. recalls Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally invasive surgery allowing access for vessel…

    A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a 0.178" difference in the end of the endoscope slot to the end of the tail piece. This allows the scope to move further into the plastic sheath…

    FDA · DeviceZimmer, Inc.NationwideOfficial notice →
  11. 2024-09-18
  12. US
    Drugs & medicalClass II

    Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or non-cemented femoral and…

    Mislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck sleeve, and vice versa. The neck of the sleeve can be…

    FDA · DeviceZimmer GmbHWorldwide distribution - US Nationwide and the countries of Japan, Netherlands.Official notice →
All 21 Zimmer recalls →

Other drugs & medical recalls in the United States

  1. 2025-03-26
  2. US
    Drugs & medicalClass II

    Rising Pharma Holding, Inc. recalls Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ…

    CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.

    FDA · DrugRising Pharma Holding, Inc.Nationwide in the USA.Official notice →
  3. 2025-03-20
  4. US
    Drugs & medical

    Woolite Delicates Detergent Recalled by Reckitt Due to Risk of Exposure to Bacteria; Sold Exclusively on Amazon.com

    The recalled products can contain Pseudomonas species bacteria, including Pseudomonas oleovorans, an environmental organism found widely in soil and water. People with weakened immune systems or external medical…

    CPSCReckitt Benckiser LLC, of Parsippany, New JerseyAbout 16,200Official notice →
  5. 2025-03-19
  6. US
  7. US
    Drugs & medicalClass II

    Stryker Corporation recalls Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197

    Increase in complaints concerning "pullwire" breakage that may result in the broken pullwire remaining in the anchor implant body after deployment.

    FDA · DeviceStryker CorporationWorldwide - US Nationwide distribution including in the states of Alabama,…Official notice →
  8. US
    Drugs & medicalClass II

    Spectrum Medical Inc recalls Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pump, Blood, Cardiopulmonary Bypass,…

    Their is a potential of fluid leakage from the centrifugal blood pump pump during the priming procedure or during clinical procedures.

    FDA · DeviceSpectrum Medical IncUS Nationwide distribution including in the states of Alabama, Arizona,…Official notice →
  9. US
    Drugs & medicalClass II

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

    The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin freely within the idler pulley housing. When the problem occurs, the analyzer may generate a system event for a Wash Wheel Dispense Arm Spin Mixer…

    FDA · DeviceBeckman Coulter, Inc.US Nationwide. Global Distribution.Official notice →
See all drugs & medical recalls →