The Recall Desk

Manufacturer

Zimmer, Inc.

446 recalls in our database name Zimmer, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
446
Critical
0
Severe
44
Most recent
2026-07-01

Of the 446 recalls from Zimmer, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 44 (10%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

376–400 of 446

  • ModerateFDA (Devices)·Z-0390-2013·2012-11-28

    Zimmer Recalls VerSys Provisional Femoral Heads for Surgical Technique Updates

    Zimmer, Inc. is recalling VerSys provisional femoral heads to update surgical instructions regarding the visual location of displaced heads.

    Product
    00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys Femoral Head Provisional 26mm +0 00789502603 VerSys Femoral Head Provisional 26mm +3.5 00789502604 VerSys Femoral Head Provisional 26mm +7 00789502605 VerSys Femoral Head Provisional 26mm +10.5 12/14 Ne
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0394-2013·2012-11-28

    Zimmer Recalls VerSys Provisional Femoral Heads for Surgical Technique Updates

    Zimmer, Inc. is recalling VerSys Provisional Femoral Heads to update surgical instructions regarding the visual location of displaced heads and fit issues.

    Product
    00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys Femoral Head Provisional 40mm +0 00789504003 VerSys Femoral Head Provisional 40mm +3.5 00789504004 VerSys Femoral Head Provisional 40mm +7 00789504005 VerSys Femoral Head Provisional 40mm +10.5 The prov
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0386-2013·2012-11-28

    Zimmer Recalls Trilogy Longevity Constrained Liners Due to Packaging Error

    Zimmer, Inc. is recalling Trilogy Longevity Constrained Liners because they were packaged in incorrect cartons, although the product labels are correct.

    Product
    Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves as the articular surface for a femoral head in total hip arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0296-2013·2012-11-21

    Zimmer Recalls ATS 3000 Tourniquets Due to Counterfeit Chip Failures

    Zimmer is voluntarily removing 204 ATS 3000 Automatic Tourniquet Systems worldwide after complaints of failures caused by counterfeit chips.

    Product
    ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended to be used by qualified medical professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0217-2013·2012-11-14

    Zimmer MS-30 Stem Recall for Patient Label Discrepancies

    Zimmer Inc. is correcting patient labels for MS-30 Stems manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    MS-30¿ Stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0235-2013·2012-11-14

    Zimmer Recalls Mueller Low Profile Cups Due to Label Discrepancies

    Zimmer Inc. is correcting patient labels for Mueller Low Profile Cups manufactured before March 2010 due to reference and lot number discrepancies.

    Product
    Original M.E. Mueller" Low Profile Cup Sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0239-2013·2012-11-14

    Zimmer Recalls Dynesys Revision Set Screws Due to Label Discrepancies

    Zimmer Inc. is correcting patient labels for Dynesys Revision set screws manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Dynesys¿ Revision + set screw
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0212-2013·2012-11-14

    Zimmer Recalls BioloX Option Ceramic Femoral Heads Due to Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for BioloX Option Ceramic Femoral Head Systems manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Biolox¿ Option Ceramic Femoral Head System Rx, sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0240-2013·2012-11-14

    Zimmer Recalls Dynesys HA Pedicle Screws Due to Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for Dynesys HA Pedicle screws manufactured before March 2010 due to reported discrepancies between product and patient labels.

    Product
    Dynesys¿ HA Pedicle + set screw
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0232-2013·2012-11-14

    Zimmer Anatomical Shoulder Ball Taper Label Correction

    Zimmer Inc. is correcting patient labels for Anatomical Shoulder Ball Tapers due to discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Ball taper for humeral stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0228-2013·2012-11-14

    Zimmer Inverse/Reverse Screw System Label Correction

    Zimmer, Inc. is correcting patient labels for Inverse/Reverse Screw systems manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Zimmer Inverse/Reverse Screw system,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0249-2013·2012-11-14

    Zimmer MS-30 Sterile Shafts Recalled for Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for MS-30 Sterile Shafts due to discrepancies in reference and lot numbers.

    Product
    MS-30 Shaft, Sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0227-2013·2012-11-14

    Zimmer Inc. Recalls Anatomical Shoulder Humeral Stems Due to Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for Anatomical Shoulder Humeral stems manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Revision Humeral stem,7,9,12,14 and Anatomical Shoulder Fracture Humeral stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0213-2013·2012-11-14

    Zimmer Recalls Wagner SL Revision Stems for Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for Wagner SL Revision Stems due to discrepancies in reference and lot numbers.

    Product
    Wagner SL Revision Stem, uncemented Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0247-2013·2012-11-14

    Zimmer Recalls Tibia Intramedullary Nails Due to Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for Sirus intramedullary nails for tibia due to discrepancies in reference and lot numbers.

    Product
    Sirus¿ intramedullary nail for tibia, cannulated ¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0238-2013·2012-11-14

    Zimmer Recalls Dynesys Stabilizing Cords Due to Labeling Discrepancies

    Zimmer, Inc. is correcting patient labels for Dynesys L.I.S. Stabilizing Cords manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Dynesys¿ L.I.S. Stabilizing cord Rx, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0210-2013·2012-11-14

    Zimmer Recalls Alloclassic SL Shafts for Labeling Discrepancies

    Zimmer, Inc. is correcting patient labels for Alloclassic SL Shafts manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Alloclassic SL Shaft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0233-2013·2012-11-14

    Zimmer Anatomical Shoulder Fracture Humeral Head Label Correction

    Zimmer, Inc. is correcting patient labels for 26 Anatomical Shoulder Fracture Humeral Head units due to discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Fracture Humeral Head
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0211-2013·2012-11-14

    Zimmer Recalls Ceramic Femoral Heads Due to Label Discrepancies

    Zimmer Inc. is correcting patient labels for Biolox delta Ceramic Femoral Heads manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Biolox¿ delta Ceramic Femoral Head Rx only, sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0237-2013·2012-11-14

    Zimmer Recalls Dynesys Universal Spacers Due to Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for Dynesys Universal Spacers manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Dynesys¿ Universal spacer 6-45
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0231-2013·2012-11-14

    Zimmer Recalls Shoulder Humeral Inserts Due to Label Discrepancies

    Zimmer Inc. is correcting patient labels for 74 anatomical shoulder humeral inserts manufactured before March 2010 due to reported discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide