Recall archive
31,892 recalls · page 403 of 1329
Reported Aug 17, 2022
Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glenmark Pharmaceuticals Inc., USA
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 17, 2022
HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1-inch needle} 200 pieces/box. Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Guangdong Haiou Medical Apparatus Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 17, 2022
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type
High riskUsing this product could cause serious injury, illness or death — stop using it now.Haimen Shengbang Laboratory Equipment Co. Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manufactured by West-Ward Eatontown, NJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hikma Pharmaceuticals USA Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 17, 2022
Triple Antibiotic Ointment, Bacitracin zinc, Neomycin sulfate, Polymixin B sulfate, First Aid Antibiotic, Triple…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical-Surgical Inc. Corporate Office
16 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 17, 2022
3D Systems VSP Reconstruction, Model: VSPR-301 Product: Scapula Marking Guide (Anatomically Shaped), Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Modeling, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Cobalt Implantable Cardioverter Defibrillators: a. Cobalt XT VR ICD, Model Numbers: DVPA2D1, DVPA2D4; b. Cobalt XT DR…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nature's Sunshine Products
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 17, 2022
ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Refresco Beverages US Inc.
FDA (openFDA food enforcement)
Reported Aug 17, 2022
cobas e801 Immunoassay Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Organic Amaranth, item # 4602, packaged in 25kg and supersack totes. Product is raw grain and imported from India.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smirks Ltd.
FDA (openFDA food enforcement)
Reported Aug 17, 2022
Xhibit Telemetry Receiver, Model: 96280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
FentaNYL Citrate in 0.9% Sodium Chloride 1 mg per 100 mL (10 mcg per mL) IV bags, Rx only, SterRx, 141 Idaho Ave.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SterRx, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 17, 2022
Prednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd., Bengaluru -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Strides Pharma Inc.
FDA (openFDA drug enforcement)
Reported Aug 17, 2022
Azacitidine for Injection 100mg/vial Lyophilized Powder, Rx Only, Mfd. in Romania By: Sindan Pharma SRL For BluePoint…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Aug 16, 2022
Lyons Magnus LLC recalls Lyons, Barista, Ready Care, various Nutritional and beverage products due to Due to the potential for microbial contamination,…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Lyons Magnus LLC
FDA (recalls & safety alerts)
Consumer productsReported Aug 15, 2022
4moms Recalls More than 2 Million MamaRoo and RockaRoo Infant Swings and Rockers Due to Entanglement and Strangulation…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thorley Industries, LLC, d.b.a. 4moms
CPSC
Reported Aug 14, 2022
Home Run Inn Frozen Foods Recalls Frozen Meat Pizza due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Woodridge 31 Copacking Company LLC
USDA FSIS
Consumer productsReported Aug 11, 2022
Future Motion Recalls Footpads for Onewheel GT Electric Skateboards Due to Bystander Injury Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Future Motion Inc.
CPSC
Consumer productsReported Aug 11, 2022
Residential Elevators Recalls Home Elevators Due to Child Entrapment Hazard; Risk of Serious Injury or Death to Young…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Residential Elevators, Inc.
CPSC
Reported Aug 10, 2022
PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
EkoSonic Kit 135cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Craftmatic Model 1 Base for Dual Bed Configurations
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Craftmatic Industries, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
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