Recall archive
245 recalls · page 1 of 11
Reported Aug 12, 2026
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand · Reason for recall — Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile…
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2026
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Product · Product details · Reason for recall — Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health…
1 more product in this recall
FDA (openFDA device enforcement)
Consumer productsReported Jul 9, 2026
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sold Exclusively on Amazon.com by BBRKIN
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jomani International Inc.
Matched: Product · Product details · Reason for recall — The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
CPSC
Reported Nov 12, 2025
Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with: Biomet 3i" Certain 3.4/4.1/5.0/6.0 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prismatik Dentalcraft, Inc.
Matched: Product · Product details — Incorrect titanium screw, packaged with dental implant.
FDA (openFDA device enforcement)
Reported Nov 12, 2025
Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
Matched: Product · Product details · Reason for recall — 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…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2025
BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand · Product · Product details — There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
FDA (openFDA device enforcement)
Reported Oct 1, 2025
Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand — 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 (openFDA device enforcement)
Reported Jun 25, 2025
Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preat Corp.
Matched: Product · Product details — Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter…
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +0 Neck, Model Number 802602202; Prosthesis, Hip,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
Matched: Product · Product details — The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with…
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2024
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand — Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find…
FDA (openFDA device enforcement)
Reported Jul 3, 2024
RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand — 41 mm acetabular outer heads were potentially assembled with a 42 mm locking ring, may lead to joint instability leading requiring surgical…
FDA (openFDA device enforcement)
Consumer productsReported Jun 6, 2024
SA Consumer Products Recalls Sanctuary Quick Access and Sports Afield Biometric Gun Safes Due to Serious Injury Hazard…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SA Consumer Products Inc.
Matched: Product · Product details · Reason for recall — The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
CPSC
Reported May 1, 2024
Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand — Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.
FDA (openFDA device enforcement)
Reported May 1, 2024
Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ebi, LLC
Matched: Product · Product details — Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being…
3 more products in this recall
FDA (openFDA device enforcement)
Consumer productsReported Feb 22, 2024
Bulldog Cases Recalls Biometric Gun Safes Due to Serious Injury Hazard and Risk of Death
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bulldog Cases
Matched: Product · Product details · Reason for recall — The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death if the safe is used to…
CPSC
Consumer productsReported Feb 22, 2024
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sold Exclusively on Amazon.com by BBRKIN
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jomani International Inc.
Matched: Product · Product details · Reason for recall — The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
CPSC
Consumer productsReported Feb 22, 2024
Machir Recalls Biometric Personal Safes Due to Serious Injury Hazard and Risk of Death
High riskUsing this product could cause serious injury, illness or death — stop using it now.Machir LLC
Matched: Product · Product details · Reason for recall — The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death if the safe is used to…
CPSC
Consumer productsReported Feb 22, 2024
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Imported by Awesafe
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shenghaina Technology Co. Ltd., d/b/a Awesafe
Matched: Product · Product details · Reason for recall — The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death.
CPSC
Reported Jan 10, 2024
Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet Spine Inc.
Matched: Brand — Spinal fixation system 7.5mmx 50mm screws are packaged with the correct labeling, but the screws themselves were laser marked with an incorrect size…
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Biolox Ceramic Option Head Zimmer 12/14 40mm -3, Item Number 00-8777-040-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand — 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…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand — Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in…
18 more products in this recall
FDA (openFDA device enforcement)
Consumer productsReported Oct 19, 2023
Fortress Safe Announces Recall of Biometric Gun Safes Due to Serious Injury Hazard and Risk of Death; One Death Reported
High riskUsing this product could cause serious injury, illness or death — stop using it now.Xpedition LLC, dba Fortress Safe
Matched: Product · Product details · Reason for recall — The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
CPSC
Reported Jul 26, 2023
MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materialise N.V.
Matched: Product · Product details — The wrong tibia guide was included intended for a different patient case.
FDA (openFDA device enforcement)
Reported Mar 29, 2023
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
Matched: Brand — The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
FDA (openFDA device enforcement)
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