Recall archive
31,892 recalls · page 238 of 1329
Consumer productsReported Jul 3, 2024
Focusee Recalls Tideway Hair Dryers Due to Electrocution or Shock Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Focusee Ltd.
CPSC
Reported Jul 3, 2024
Fresh Catch Inc. Yellowfin Tuna, 1 loin per case packaged in carboard boxes with keep refrigerated label
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Catch Inc.
FDA (openFDA food enforcement)
Reported Jul 3, 2024
CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 5865770-01054696; e)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare Finland Oy
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Global Mix Inc.
FDA (openFDA food enforcement)
Reported Jul 3, 2024
Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, a) 30 capsules bottles, NDC 60429-165-30; b) 90 capsules…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Medical Supply Inc.
FDA (openFDA drug enforcement)
Reported Jul 3, 2024
Green Life Farms Baby Arugula in 4.5 ounce plastic clamshell packaging containers. 6 packages per case of 4.5oz each.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Green Life Farms
FDA (openFDA food enforcement)
Consumer productsReported Jul 3, 2024
Hatch Baby Recalls Power Adapters Sold with Rest 1st Generation Sound Machines Due to Shock Hazard
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hatch Baby Inc.
CPSC
Reported Jul 3, 2024
Inspire Model 3028, IV Implantable Pulse Generator
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inspire Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2024
CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Chef Select 2 Garlic Baguettes filled With Garlic Butter 2x175 g Barcode: 4056489447559. Frozen product packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lidl US TRADING
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 3, 2024
The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
22 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Prelude Roadster Guide Sheath REF: -PG4F45S -PG4F90S -PG5F45MP -PG5F45R -PG5F45S -PG5F45S018 -PG5F90MP -PG5F90S…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2024
The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6 French. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mermaid Medical A/S
FDA (openFDA device enforcement)
Reported Jul 3, 2024
SinuFrin Decongestant (oxymetazoline HCl) Nasal Solution Nasal Decongestant, Decongestant Relief for up to 12 Hours, 12…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Neilmed Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jul 3, 2024
NovaGuide 2 Intelligent Ultrasound, REFs: NSC-NVGSYS2 & NSC-NVGSYS2-CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NovaSignal Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Zilretta (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacira Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jul 3, 2024
"THE PERFECT CHOCOLATE CHUNK COOKIE MIX Cravings by Chrissy Teigen NET WT. 15.76 OZ (447g)" Packaged in a beige…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penguin Natural Foods, Inc.
FDA (openFDA food enforcement)
Reported Jul 3, 2024
Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 3, 2024
SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips North America LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2024
Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Consumer productsReported Jul 3, 2024
SWOMOG Children's Pajamas Recalled Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold Exclusively…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ShenZhen Bai Si Te Clothing Limited Company, dba SWOMOG
CPSC
Reported Jul 3, 2024
Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Siemens Material Number: 11416751 RAPIDPoint 500e Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2024
AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
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