Recall archive
32,165 recalls · page 474 of 1341
Reported Dec 1, 2021
The da Vinci Xi and X surgical systems (IS4000 and IS4200) each consist of three main components: the Surgeon Console…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Kings Hawaiian Hawaiian Sweet Hamburger Buns8 buns NET WT 12.8 oz. (362.9 g) UPC 0 73435-06050 Product Number 800020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King's Hawaiian Bakery
FDA (openFDA food enforcement)
Reported Dec 1, 2021
MaryRuth's Organic Infants Liquid Probiotic; Unflavored, a Dietary Supplement. 1 fl. oz. (30 mL) UPC: 8 56645 00858 7…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mary Ruth Organics
FDA (openFDA food enforcement)
Reported Dec 1, 2021
Medtronic CareLink SmartSync Device Manager application software (D00U005) used by the following Medtronic Cobalt and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Medtronic Wireless Recharger Model WR9220 included in the RS5200 Recharger Kit used by the InterStim Micro (Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Cardioblate CryoFlex Surgical Ablation Console
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - CT Vision ACQSIM CT System Number: 728209 Continuous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
SOMATOM Force with software syngo.CT VB20 Model #10742326
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
16 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Diclofenac Sodium Topical Solution USP, 1.5 w/w, 5 fl oz (150 mL) plastic bottles, Rx only, Teligent Pharma, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teligent Pharma, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Dec 1, 2021
Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Garden Side Salad 6.95oz. (197g) UPC:72251525202. Packaged in plastic containers.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ukrop's Homestyle Foods, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 1, 2021
Topiramate Tablets, USP 50 mg, 500-count bottles, Rx Only, Manufactured by: Unichem Laboratories LTD, Ind. Area. Meerut…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Unichem Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Dec 1, 2021
Roberts Digital VIPR System (with E-size cylinder) Model: ROC-9840
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western/Scott Fetzer Company
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 24, 2021
Flocinolone Acetonide 0.01% Topical Oil, Body Oil, Rx, packaged in 4 oz. bottle, Distributed by: Amneal Pharmaceuticals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amneal Pharmaceuticals
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 24, 2021
Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-12709-WC The…
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 Nov 24, 2021
LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Healthcare Pharmaceuticals Inc.
18 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 24, 2021
Beaver Xstar Crescent Knife, 2.5mm, 55 degrees, bevel down. Intended for or cataract surgery. REF#: 373809
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec International, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 24, 2021
BIO-RAD BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack The BioPlex Syphilis Total & RPR kit is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 24, 2021
API 50 CH, Model 50300
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Nov 24, 2021
Raw onion sold in bags or sliced and diced with the following item numbers and lot code. 1. RED JUMBO 25# 1/25 LB, item…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bix Produce Company LLC
FDA (openFDA food enforcement)
Reported Nov 24, 2021
5 lb. boxes of yellow onions packaged in cardboard boxes
High riskUsing this product could cause serious injury, illness or death — stop using it now.Brothers Produce
FDA (openFDA food enforcement)
Reported Nov 24, 2021
Carolina Ingredients Beef Gravy Mix Non-allergen N715025 Net Wt. 50 lbs. Mfr. By: Carolina Ingredients, LLC Rock Hill,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carolina Ingredients
5 more products in this recall
FDA (openFDA food enforcement)
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