Recall archive
32,165 recalls · page 496 of 1341
Reported Aug 25, 2021
ECHELON FLEX Powered Plus Stapler-intended for transection, resection, and/or creation of anastomoses. The instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Cholestene capsules, 1200 mg of red yeast rice per 2 capsules, 120-count bottle, Manufactured by: High Performance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.High Performance Formulas, LLC (HPF, L.L.C.)
FDA (openFDA drug enforcement)
Reported Aug 25, 2021
Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation during robotic/non-robotic intra-operative and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Healthcare Americas Corporation
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Triathlon Prim CEM FXD BPLT 7, Catalog No. 5520B700
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Flavored Bacon Ranch Seasoning Packaged in 25lb kraft paper bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mane Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 25, 2021
GaviLyteTM - C PEG-3350 (240g) and Electrolytes for Oral Solution, USP with Flavor Pack Manufactured by Novel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novel Laboratories, Inc. d.b.a LUPIN
FDA (openFDA drug enforcement)
Reported Aug 25, 2021
Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg per day, 50/140 Twice Weekly, Rx Only a) 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noven Pharmaceuticals Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 25, 2021
Soltive Premium Super Pulsed Laser System (TFL-PLS) & Pro Super Pulsed Laser System (TFL-SLS). Intended for incision,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Aug 25, 2021
OPTI SARS-CoV-2 RT-PCR Test, REF Numbers: a) 99-57003 b) 99-57004
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OPTI Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
CIRCUL8 LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF: 08-0020, Rx Prescription Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho8, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
FLASH Ostial System, Dual Balloon Angioplasty Catheter, REF: OAB6014BA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ostial Corporation
FDA (openFDA device enforcement)
Reported Aug 25, 2021
728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance iCT Upgrades
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 Aug 25, 2021
Trilogy Evo, Product numbers BL2110X15B, CA2110X12B, DE2110X13B, DS2110X11B, EE2110X15B, ES2110X15B, EU2110X15B,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Respironics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Consumer productsReported Aug 25, 2021
Razor USA Recalls GLW Battery Packs Sold with Hovertrax 2.0 Self-Balancing Hoverboards Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Razor USA LLC
CPSC
Reported Aug 25, 2021
Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spirit Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Aug 25, 2021
Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufacturer T&R Enterprises St. Louis MO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.T & R Enterprises USA, Inc.
FDA (openFDA food enforcement)
Reported Aug 25, 2021
RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Europe Ltd.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Econazole Nitrate Cream 1%, 85 grams bulk shippers, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC…
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 Aug 25, 2021
DAUNOrubicin Hydrochloride Injection 20 mg/4mL, 4mL Single Dose vials, 10 in 1 carton, Rx only, Teva Parenteral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
18 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 25, 2021
The Aequalis Pyrocarbon Humeral Heads. Shoulder implant component. Sold OUS only: a) Catalog # DWH039 - Diameter 39 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier S.A.S.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Gore Propaten Vascular Graft configured for Pediatric Shunt, Diameter 5 mm, Length 10 cm, Rx Only, Sterile EO, for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Consumer productsReported Aug 25, 2021
Wee Gallery Recalls Wooden Tray Puzzles Due to Choking Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wee Gallery
CPSC
Reported Aug 25, 2021
Carvedilol Tablets, USP 25 mg, 500 Tablets bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., India,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals (USA) Inc.
FDA (openFDA drug enforcement)
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