Recall archive
31,892 recalls · page 248 of 1329
Reported May 29, 2024
Brand Name: MEDLINE Product Name: SYR 30ML/LS Model/Catalog Number: 83077 Product Description: NON-Sterile syringes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jiangsu Shenli Medical Production Co., Ltd.
86 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2024
chuao CHOCOLATIER potato chip mini chocolate bar, 0.39oz/11g
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Kairo's Group, Inc. dba Chuao Chocolatier
FDA (openFDA food enforcement)
Reported May 29, 2024
Bulk flour tortillas sold to food service. 20ct 6in flour. 12 packages of 20ct per case. Packed in clear plastic bag…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.La Original Tortilla Co., Inc.
FDA (openFDA food enforcement)
Reported May 29, 2024
Prelude Guide Sheath Roadster, REF PG5F45S018, 5F 0.076 (1.9 mm), 45 cm, STERILE EO, RX ONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 29, 2024
Mucci Food Products, Ltd. Tiramisu Italian Dessert, 2, 4.25 lb trays per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mucci Food Products, Ltd. dba Mama Mucci's Pasta
FDA (openFDA food enforcement)
Reported May 29, 2024
Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code: 6 32565 00004 3 Bottle UPC Code: 6 32565 00001 2
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Natural Waters
FDA (openFDA food enforcement)
Reported May 29, 2024
InstaClear Lens Sheath. The InstaClear lens cleaner system and versatile sheath cleans and clears the lens of a rigid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported May 29, 2024
Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump
High riskUsing this product could cause serious injury, illness or death — stop using it now.OptumHealth Care Solutions LLC
FDA (openFDA device enforcement)
Reported May 29, 2024
Achieva 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
31 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2024
BiPAP V30 Auto Ventilator, Part Number 1111178
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2024
Duloxetine Delayed-Release Cap USP 30mg, 30-count bottle, Rx only, Preferred Pharmaceutcals, Inc., NDC 68788-9301-03
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported May 29, 2024
Product is MACARONI Salad, but the bottom container is mislabeled with the ingredients statement for COLESLAW. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reser's Fine Foods, Inc.
FDA (openFDA food enforcement)
Reported May 29, 2024
Sagent Pharmaceuticals recalls Sagent Docetaxel Injection, USP due to Potential presence of particulate matter
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Sagent Pharmaceuticals
FDA (recalls & safety alerts)
Reported May 29, 2024
IMMULITE 2000 Anti-TG Ab Catalog # L2KTG2 (200 Tests), SMN 10381659, System, Test, Thyroid Autoantibody.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 29, 2024
Haloperidol decanoate Injection 50mg/mL, packaged in a) 1 mL Single-Dose Vials (NDC 70069-381-01) and b) 10 1mL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Somerset Therapeutics LLC
FDA (openFDA drug enforcement)
Reported May 29, 2024
8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a next-generation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Leibinger GmbH & Co. KG
FDA (openFDA device enforcement)
Reported May 29, 2024
Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only, Manufactured by: Sun…
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 May 29, 2024
Queso de mano, Fresh soft white cheese, NET WT 24 oz.(640g), Keep Refrigerated, plastic container, packed 12 plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tama Corporation
FDA (openFDA food enforcement)
Reported May 29, 2024
Stryker Blueprint Software, Catalog #BPUE001.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier S.A.S.
FDA (openFDA device enforcement)
Reported May 29, 2024
Wegman's Half Loaf Garlic Bread
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
FDA (openFDA food enforcement)
Reported May 29, 2024
Yamaha Surface Mounter YR series, YS series, i-Pulse series, Sigma series, S series, M series. Affected models: YSM10,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Yamaha Motor Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2024
Dairy Manufacturers Inc. recalls Crecelac and Farmalac Infant Formula due to Food Compliance Programs – Baby Formula
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Dairy Manufacturers Inc.
FDA (recalls & safety alerts)
Reported May 24, 2024
AMB Food Inc recalls Pop a Nosh Mixed Munch Regular and Honey BBQ due to Undeclared allergen - wheat
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.AMB Food Inc.
FDA (recalls & safety alerts)
Consumer productsReported May 23, 2024
TOPINCN Pool Drain Covers Recalled Due to Entrapment Hazard; Violation of the Virginia Graeme Baker Pool and Spa Safety…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dong Guan Shi Li Peng Zhi Dian Zi Shang Wu You Xian Gong Si, dba Sanure Storefront
CPSC
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