Recall archive
31,892 recalls · page 216 of 1329
Reported Oct 2, 2024
Stryker TMJ Unilateral Implant, REF: GHG010, consisting of the following components: Ref: CHG010AM, Anatomical Bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TMJ Solutions Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Vivier Sheer SPF 30 Mineral With Antioxidants (titanium dioxide 10% and zinc oxide 8%) packaged in 60 ml/2 fl oz,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vivier Pharma, Inc.
FDA (openFDA drug enforcement)
Reported Oct 2, 2024
LINK Universal Handle, with quick coupling, Stainless Steel, straight, Item Number 130-394/01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Corp. Hq.)
FDA (openFDA device enforcement)
Reported Oct 2, 2024
GE Giraffe Warmer, Model/Catalog Number M1118179-01090979. Infant radiant warmers provide infrared heat in a controlled…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wipro GE Healthcare Private Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2024
Pork Dynasty Inc. Recalls Ready-to-Eat Fried Pork Skin Products Due to Misbranding and Undeclared Allergen
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pork Dynasty, Inc.
USDA FSIS
Consumer productsReported Sep 26, 2024
John Deere Recalls Compact Utility Tractors Due to Crash Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Deere & Company
CPSC
Consumer productsReported Sep 26, 2024
Liberty Hardware Recalls Multi-Grip Tub Safety Bars Due to Fall Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Liberty Hardware Manufacturing Corp.
CPSC
Reported Sep 25, 2024
SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Baxter EXACTAMIX Inlet, Non-Vented, High Volume Inlet, REF H938173, for use in a pharmaceutical compounding device
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Marabou Sea Salt Chocolate Bar; 185g; yellow plastic packaging and the word 'havvsalt', the Swedish word for "sea…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BonBon NYC LLC.
FDA (openFDA food enforcement)
Reported Sep 25, 2024
Flexima APDL Drainage Catheter System and Kit, Material Numbers: a) REF M001271960, b) REF M001271970; all-purpose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Btt Health GmbH
FDA (openFDA device enforcement)
Reported Sep 25, 2024
BiomarC EX Fiducial Marker System, Catalog Number 040165
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Carbon Medical Technologies, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cypress Medical Products LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Wegmans PECAN BLEND NET WT 16OZ (1LB) 453g Ingredients: Pecans, Cashews, Pistachios, Canola and/or Peanut and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flagstone Foods LLC
FDA (openFDA food enforcement)
Reported Sep 25, 2024
Supreme Peppers Tri Blend 8-50053-68534 8 OZ Supreme Jalapenos Diced 8-50053-68536 7 OZ Supreme Peppers W/Onions…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GBC Food Services, LLC dba Yummi Sushi
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 25, 2024
ViewPoint; system, imaging processing, radiological
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: a) 2110344-008; b) 2110344-009; c)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Sep 25, 2024
TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovasis, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2024
KODIAK PROTEIN-PACKED POWER WAFFLES BUTTERMILK & VANILLA NET WT 3.35 lb (53.6oz) 1.52kgCreated & distributed by: KODIAK…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kodiak Cakes LLC
FDA (openFDA food enforcement)
Reported Sep 25, 2024
Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mazor Robotics Ltd.
FDA (openFDA device enforcement)
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