Recall archive
31,892 recalls · page 315 of 1329
Reported Sep 27, 2023
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Membrane Changer Single-Use, REF MC, each package contains 3 changers; Membrane Changer Reloadable, REF MC-R, each…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SenTec AG
FDA (openFDA device enforcement)
Reported Sep 27, 2023
smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, REF 71421265; knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Somebody's Mother's White Chocolate, Net Wt 9.5 oz (270g), UPC 5803100102
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Somebody's Mother's Chocolate Sauce
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2023
Radish Turnip Cake (w/o shrimp): The product comes in a 900g ( 32 ounce), clear plastic package marked with UPC #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southern Taiwan LLC
FDA (openFDA food enforcement)
Reported Sep 27, 2023
Stryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-, Allows the user to mix bone cement with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)),…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sun Pharmaceutical Industries Inc.
FDA (openFDA drug enforcement)
Reported Sep 27, 2023
TyTek Tension Pneumothorax Access Kit TPAK 14 gauge 3.25 inch- Intended for introduction into the body to facilitate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tytek Medical Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Kroger Mint Burst ANTISEPTIC MOUTH RINSE ANTIGINGIVITIS/ANTIPLAQUE (Eucalyptol 0.092%, menthol 0.042%, Methyl…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vi-Jon, LLC
FDA (openFDA drug enforcement)
Reported Sep 25, 2023
Del Valle Import and Export, LLC, Recalls Ineligible Pork Chicharrones Product Imported From Honduras
High riskUsing this product could cause serious injury, illness or death — stop using it now.Del Valle Import and Export, LLC,
USDA FSIS
Reported Sep 23, 2023
Green Valley Foods Retira Productos Congelados De Pizza De Carne Debido A Un Error De Rotulación Y Alérgenos No…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Green Valley Foods
USDA FSIS
Reported Sep 22, 2023
Potential contamination with Bacillus cereus recalls VistaPharm Sucralfate Oral Suspension 1g/10mL due to Potential contamination with Bacillus cereus
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Potential contamination with Bacillus cereus
FDA (recalls & safety alerts)
Consumer productsReported Sep 21, 2023
FXI Recalls Novaform ComfortGrande and DreamAway Mattresses Due to Risk of Mold Exposure; Sold Exclusively at Costco…
High riskUsing this product could cause serious injury, illness or death — stop using it now.FXI Inc.
CPSC
Consumer productsReported Sep 21, 2023
DR Power Equipment Recalls DR Power Chipper Shredders Due to Laceration Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Generac Power Systems Inc.
CPSC
Consumer productsReported Sep 21, 2023
H&M Recalls Men's Clasp Beaded Bracelets Due to Lead Poisoning Hazard; High Levels of Lead Content
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.H&M Hennes & Mauritz LP
CPSC
Consumer productsReported Sep 21, 2023
HONEY JOY Recalls Infant Swings Due to Suffocation Hazard and Violation of Federal Safety Standards; Sold Exclusively…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Honey Joy Company
CPSC
Consumer productsReported Sep 21, 2023
Make Believe Ideas Recalls Seven Rainbow Road Board Books Due to Choking Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Make Believe Ideas Ltd.
CPSC
Consumer productsReported Sep 21, 2023
Shimano Recalls Cranksets for Bicycles Due to Crash Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shimano North America Bicycle Inc.
CPSC
Reported Sep 21, 2023
TAMA Corporation recalls PAISA Sweet Corn Pancakes "Cachapas de Maiz" due to Undeclared wheat and soy allergens; undeclared yellow #5
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.TAMA Corporation
FDA (recalls & safety alerts)
Reported Sep 20, 2023
Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2023
ASG-001; Ultrasound gel
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advance Medical Designs, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Welch Allyn Connex Spot Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Pantoprazole Sodium for Injection 40mg per vial, Single dose vials NDC 71839-122-01 Packaged as (a) 10 Single-dose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Be Pharmaceuticals Ag
FDA (openFDA drug enforcement)
Reported Sep 20, 2023
FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
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