Biomet Recalls
225 recalls on record in the United States
Biomet, Inc. recalls Zimmer Biomet Comprehensive Segmental Revision System (SRS).
During assembly, an SRS Humeral Distal Body implant failed to engage correctly at the point of reduction with a Discovery Elbow System Humeral Condyle. A mismatch between the screw holes in the Humeral Body & Elbow Condyle affects assembly during surgery. If the product has already been implanted, no action is required. The mismatch is estimated to prevent screw engagement in less than 1% of cases.
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Biomet Microfixation, LLC recalls Biomet Microfixation TraumaOne System Surgical Tray - Model
Part of the number on the tray lid differ from the part number on the base.
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Biomet 3i, LLC recalls BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Pla
A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Left Medial Tibial Trial Tray Siz
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Right Medial Tibial Trial Tray Si
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Right Medial Tibial Trial Tray Si
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Phase 3 Tibial Template Right Med
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Right Medial Tibial Trial Tray Si
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Phase 3 Tibial Template Right Med
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Femoral Slap Hammer Product Usag
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Left Medial Tibial Trial Tray Siz
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Left Medial Tibial Trial Tray Siz
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Phase 3 Tibial Template Left Medi
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Left Medial Tibial Trial Tray Siz
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Right Medial Tibial Trial Tray Si
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Us
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Us
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Unicompartmental Knee Phase 3 Tibial Impactor Produc
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Partial Knee System Phase 3 Tibial Template Right Med
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Phase 3 Tibial Template Left Medi
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Left Medial Tibial Trial Tray Siz
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Right Medial Tibial Trial Tray Si
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Right Medial Tibial Trial Tray Si
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Phase 3 Tibial Template Right Med
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Partial Knee System Right Medial Tibial Trial Tray Si
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
View recall details →
Biomet U.K., Ltd. recalls Oxford Knee System Tibial Resector Body Tube & Guides Pro
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet U.K., Ltd. recalls Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Us
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
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Biomet, Inc. recalls BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Mo
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
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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.
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Biomet, Inc. recalls JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 11002735
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 surgical intervention.
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Showing 30 of 225 recalls. See all →