Recalls distributed in Georgia
These notices name Georgia in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
5,116 stored notices name Georgia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported Oct 21, 2026Updated Oct 26, 2026
Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(10x65mm), 10080T(10x55mm),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SI-BONE, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis; Model/Catalog Number: VSWVH0808 and VSWVN1006 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Cranberry Chicken Salad Wedge 4.5 oz package in Wedge plastic and clear container with a plastic film sealing the top.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Freshpoint Central Florida, Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.G L Mezzetta Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Oct 20, 2026
Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safeguard US Operating LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2026
SIERRA NEVADA GRAZIERS RAW MONTEREY JACK NET WT. 8oz. (225g) ITEM 6400 Plant No. 06-325 Willows, California 95988 UPC:…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Sierra Nevada Cheese Company, Inc.
FDA (weekly enforcement report)
Reported Oct 7, 2026Updated Oct 13, 2026
McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ASP Global, LLC.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Oct 7, 2026
Apheresis Platelets, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LifeSouth Community Blood Centers, Inc.
FDA (weekly enforcement report)
Reported Oct 7, 2026Updated Oct 13, 2026
Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam, REF: S420GH/EUA, S620GH/EUA; Embosphere 700-900 micrometer 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Therapeutics, Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noxbox Ltd.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
In-Line Valve, Product Number: P5-TEE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Percussionaire Corporation
3 more products in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.