Recall archive
31,892 recalls · page 286 of 1329
Reported Jan 17, 2024
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ambu Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Baxter Flo-Rester, Disposable internal vessel occluder, distributed in the following sizes: a) Product Code 50100:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
16 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
CD11b APC: ASR, REF: 340936, and CE, REF: 333143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Big Island Candies recalls Big Island Candies Brownie Assortment due to Contains undeclared peanuts
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Big Island Candies
FDA (recalls & safety alerts)
Reported Jan 17, 2024
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Belt Technologies, Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM) installed with Model 2892 Programmer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jan 17, 2024
BrightFarms recalls BrightFarms Spinach and Salad Kits due to Potential Foodborne Illness-Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.BrightFarms
FDA (recalls & safety alerts)
Reported Jan 17, 2024
MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Tacrolimus Capsules, USP 1mg, 100-Count Bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories Limited,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Reddy's Laboratories, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jan 17, 2024
Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eban's Bakehouse LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2024
Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Garden Spot Foods, LLC.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2024
VADER pedicle system, torque wrench, Catalog Number 42-702
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Icotec Ag
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Detector H. Pylori, Catalog Number IHP-30
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Immunostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2024
1/2" Diced Tomatoes in Juice packed in 55 gallon fiber drums
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingomar Packing Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2024
Vigabatrin for Oral Solution, USP 500 mg per packet, 50 packets per box, Rx Only, Manufactured by: InvaGen…
High riskUsing this product could cause serious injury, illness or death — stop using it now.InvaGen Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jan 17, 2024
Kinjin Food Pvt. Ltd. recalls Vandevi Asafoetida Yellow Powder in 50 gram, 100 gram, 200 gram, 500 gram, and 1 kilogram packages. due to May contain undeclared…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Kinjin Food Pvt. Ltd.
FDA (recalls & safety alerts)
Reported Jan 17, 2024
Desloratadine Tablets USP 5mg a) 100 count (NDC 68180-153-01) and b) 500 count (NDC 68180-153-02) bottles, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jan 17, 2024
Medline Gown Poly W/Breath Sleeves XL AAMIK Level 4 (Eclipse gown), REF SPT-2208CS, 100/pack, Non-Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
NIM TriVantage EMG Endotracheal Tubes, Model (REF) Numbers and sizes: a) 8229706, 6.0MM ID; b) 8229707, 7.0MM ID; c)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.mo-Vis BVBA
FDA (openFDA device enforcement)
Reported Jan 17, 2024
OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model: LTF-S190-5 Used with a video system center, light…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
2 more products in this recall
FDA (openFDA device enforcement)
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