Recall archive
31,892 recalls · page 214 of 1329
Reported Oct 9, 2024
Stryker Tornier Perform Humeral System, Reversed Insert, 45%, REF DWP2393, for shoulder arthroplasty
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Oct 9, 2024
BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Young Dental Manufacturing I, LLC
FDA (openFDA device enforcement)
Reported Oct 8, 2024
FSIS Issues Public Health Alert for Ready-To-Eat Cranberry Chicken Salad Products Due to Misbranding and Undeclared…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hans Kissle Company, LLC
USDA FSIS
Reported Oct 7, 2024
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal, and Trilogy EV300 ventilators due to The use of…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Philips Respironics, Inc.
FDA (recalls & safety alerts)
Reported Oct 7, 2024
Youngtown Grape Distributors Inc recalls Happy Moose Tropical Roots and Strawberry Fields, 12 oz bottles due to Potential Foodborne Illness
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Youngtown Grape Distributors Inc.
FDA (recalls & safety alerts)
Reported Oct 4, 2024
Jack and the Green Sprouts, Inc. recalls Jack & the Green Sprouts Alfalfa and Alfalfa & Onion Sprouts due to Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Jack and the Green Sprouts, Inc.
FDA (recalls & safety alerts)
Reported Oct 4, 2024
Lunds & Byerlys recalls L&B Lone Star Dip due to Potential mold contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Lunds & Byerlys
FDA (recalls & safety alerts)
Reported Oct 3, 2024
Hammond’s Candies recalls Hammond’s Dark Chocolate Filled Mini Waffle Cones due to Undeclared Milk
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hammond’s Candies
FDA (recalls & safety alerts)
Reported Oct 2, 2024
Refresh P.M., (Mineral Oil 42.5%, White Petrolatum 57.3%) Lubricant Eye Ointment, Net wt, 0.12 oz (3.5g) Tube,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AbbVie Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 2, 2024
PACEMAKER PACK, SLCV01J; Medical convenience kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ARROW INTERNATIONAL Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Mycophenolic Acid Delayed-Release Tablets USP, 360 mg, Rx Only, 120 Tablets per bottle, Manufactured by Alkem…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
FDA (openFDA drug enforcement)
Reported Oct 2, 2024
Montreal Fudge brand Chocolate Fudge with Nuts; 5.6oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Authentik Fudge
FDA (openFDA food enforcement)
Reported Oct 2, 2024
Bacalaitos Criollos, CODFISH FRYING MIX, 7 oz., packaged in a plastic bag, 24 packages (units) per cases of 7 onz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avole, Inc.
FDA (openFDA food enforcement)
Reported Oct 2, 2024
BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 The Magnum Biopsy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2024
BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
WALLFLEX FC ESO STENT RMV 18X103MM- Wallflex Esophageal Partially Covered (PC) and Fully Covered (FC) Stent System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
30 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
(a) CardinalHealth Salem Sump Dual Lumen Stomach Tube, 12 Fr/Ch (4.0 mm) x 48 in. (122 cm), Model #8888264929, Sterile;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centinel Spine, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Biodesign Fistula Plug C-FPB-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Biotech, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Silver-Plated Copper Sims Uterine Sound, Part Number 64-600
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Datascope Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Custodiol HTK Solution, 500ml bottle. 10 per carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr Franz Koehler Chemie GmbH
FDA (openFDA device enforcement)
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