Recall archive
31,892 recalls · page 205 of 1329
Reported Nov 13, 2024
MyChai Chai Tea Concentrate Original. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.My Chai Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2024
Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 and administer supplemental oxygen,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Aunt Millie s Bakehouse Hawaiian Hamburger Buns 4.5" Sliced 3 OUNCE. 6 unlabeled 12CT PKGS per sale unit case, product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Perfection Bakeries LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2024
SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and fluoroscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Corporation Medical Systems Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2024
epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System, SMN 10736515
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Tandem Intl Bipolar Cocr Shell/UHMWPE Liner, TI-6AL-4V Retaining Ring, 28MM I.D. 46 MM O.D., REF 71324046, sterile,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Staska Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Nov 13, 2024
Dapsone Gel 7.5%, 60 gram pump, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viona Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Nov 13, 2024
Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally invasive surgery allowing access…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2024
Gilster Mary Lee Corporation recalls Bowl & Basket Onion Soup Mix due to Undeclared egg
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Gilster Mary Lee Corporation
FDA (recalls & safety alerts)
Reported Nov 8, 2024
CIBUS Fresh recalls CF, J&O and other Autumn Turkey Sandwiches due to Potential Foodborne Illness – Listeria monocytogens
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.CIBUS Fresh
FDA (recalls & safety alerts)
Reported Nov 8, 2024
Wegmans Food Markets recalls Wegmans Food Markets Asian Sesame Salad with Chicken & Asian Dressing due to Potential or Undeclared Allergen – Egg
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Wegmans Food Markets
FDA (recalls & safety alerts)
Consumer productsReported Nov 7, 2024
Quad Lock MAG Battery Pack Recalled Due to Fire Hazard; Imported by Quad Lock
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Annex Products Pty Ltd., dba Quad Lock
CPSC
Consumer productsReported Nov 7, 2024
Baofali Crib Bumpers Recalled Due to Suffocation Hazard; Violation of Federal Ban on Crib Bumpers; Sold Exclusively on…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Baofali Trading Co. Ltd., dba Unique Person Home Goods
CPSC
Consumer productsReported Nov 7, 2024
Dreamgro Recalls Lullaby Travel Soothers Due to Choking Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.DreamGro Enterprises LLC
CPSC
Consumer productsReported Nov 7, 2024
GoveeLife and Govee Smart Electric Space Heaters Recalled Due to Fire and Burn Hazards; Imported by Govee
High riskUsing this product could cause serious injury, illness or death — stop using it now.Govee Moments Trading Limited, of China and Govee Moments Limited
CPSC
Consumer productsReported Nov 7, 2024
Guava Family Recalls Roam Strollers Due to Fall and Injury Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Guava Family Inc.
CPSC
Consumer productsReported Nov 7, 2024
Kyte Baby Recalls Slumber Suits Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold Exclusively on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kyte Baby
CPSC
Consumer productsReported Nov 7, 2024
Tala North America Recalls Battery Powered Portable Lamps Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tala North America Inc.
CPSC
Consumer productsReported Nov 7, 2024
Wolf Appliance Recalls Dual Fuel Ranges with Infrared Griddles Due to Burn and Fire Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wolf Appliance Inc.
CPSC
Reported Nov 6, 2024
Abbott Alinity m HPV AMP Kit, used with the Alinity m System, product codes: a) REF 09N15-095; b) REF 09N15-090; c) REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2024
Cinacalcet Tablets 30 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-440-10, b) 90 Tablets per bottle, NDC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accord Healthcare, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 6, 2024
AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accriva Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 6, 2024
Ambu¿ VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ambu Inc.
FDA (openFDA device enforcement)
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