Recall archive
31,892 recalls · page 310 of 1329
Reported Oct 13, 2023
Don Miguel Foods Recalls Frozen Ready-To-Eat Carne Asada Burrito Products Due to Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Don Miguel Mexican Foods, Inc.
USDA FSIS
Reported Oct 12, 2023
Betty Lou’s Inc. recalls Stabilyze Dark Chocolate Peanut Butter nutrition bar due to Undeclared sesame - Allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Betty Lou’s Inc.
FDA (recalls & safety alerts)
Consumer productsReported Oct 12, 2023
Family Health Products Recalls Crystal Clear Sodium Hydroxide Products Due to Failure to Meet Child-Resistant Packaging…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Family Health Products Inc., Omaha, Nebraska
CPSC
Consumer productsReported Oct 12, 2023
Countertop Nugget Ice Makers Recalled Due to Laceration Hazard ; Sold Exclusively through Amazon; Distributed by Far…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Far Success Trading Limited
CPSC
Consumer productsReported Oct 12, 2023
Little Sleepies Recalls Sleepyhead Loveys and Bandana Bibs Due to Choking Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Little Sleepies
CPSC
Consumer productsReported Oct 12, 2023
The FORT Recalls Children's Play Tents Due to Choking and Laceration Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Simulated Wood Grain Design LLC, d/b/a The FORT
CPSC
Consumer productsReported Oct 12, 2023
YourHealthToolkit Recalls Children's Weighted Blankets Due to Asphyxiation Hazard; Sold Exclusively on Amazon.com…
High riskUsing this product could cause serious injury, illness or death — stop using it now.YourHealthToolkit LLC
CPSC
Reported Oct 11, 2023
API3200MD Mass Spectrometer, Part Number 4466230
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AB Sciex, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 11, 2023
HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amerisource Health Services LLC
FDA (openFDA drug enforcement)
Reported Oct 11, 2023
Apellis Injection Kit 29g Injection Needle -single use intended to inject fluids into, or withdraw fluids from, parts…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apellis Pharmaceuticals, Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARROW INTERNATIONAL Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Belt Technologies, Inc.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM, Catalog number H965100420, cardiac guide catheter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
15 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 11, 2023
The Crooked Row - Nkratable 4.5g per bite - 3 bites per pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cannihelp Hemp Co. LLC dba The Crooked Row
FDA (openFDA food enforcement)
Reported Oct 11, 2023
fentaNYL in 0.9% sodium chloride, 10 mcg/1 mL, (10 mcg/mL), 3 mL syringe, Rx only, Central Admixture Pharmacy Services,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Central Admixture Pharmacy Services Inc.
31 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 11, 2023
Puritan Bennett Cuff Pressure Manager, REF: 180-03
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Oct 11, 2023
LFS Flat screen arm system with surgical lamp for Models Aurora series, Aurora 2 series, Aurora 3 series, Aurora 4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DKK Dai-Ichi Shomei Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Dr. Berne's MSM DROPS 15% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Berne's Whole Health Products
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 11, 2023
Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial, Rx Only, For…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eugia US LLC
FDA (openFDA drug enforcement)
Reported Oct 11, 2023
F2-01 Frame, physiological patient monitor (with arrhythmia detection or alarms)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems China Co., Ltd.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Medical Systems, Israel Ltd.
FDA (openFDA device enforcement)
Reported Oct 11, 2023
Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
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