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.
5,120 stored notices name Georgia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported May 28, 2025
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8"…
High riskUsing this product could cause serious injury, illness or death — stop using it now.C.R. Bard Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 28, 2025
Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported May 28, 2025
Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in cans, packed 12 cans per case. UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vietti Acquisitions, LLC
FDA (openFDA food enforcement)
Reported May 21, 2025
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported May 21, 2025
FoundationOne Companion Diagnostic (F1CDx)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Foundation Medicine, Inc.
FDA (openFDA device enforcement)
Reported May 21, 2025
TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 21, 2025
MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nipro Renal Soultions USA, Corporation
FDA (openFDA device enforcement)
Reported May 21, 2025
Enterprise 1.5T, Model Number: 781145;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
13 more products in this recall
FDA (openFDA device enforcement)
Reported May 21, 2025
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf GmbH
FDA (openFDA device enforcement)
Reported May 14, 2025
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ambu Inc.
FDA (openFDA device enforcement)
Reported May 14, 2025
GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in percutaneous fluid aspirations and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 14, 2025
Artix MT Thrombectomy Device, REF: 32-102
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inari Medical - Oak Canyon
FDA (openFDA device enforcement)
Reported May 14, 2025
Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported May 14, 2025
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported May 7, 2025
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported May 7, 2025
myQA iON; Article Number: MQ10-000;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IBA Dosimetry GmbH
FDA (openFDA device enforcement)
Reported May 7, 2025
Enhanced Verify Evaluation Handset (CFN HH90130FA)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported May 7, 2025
Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectrum Medical Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 7, 2025
Distal Femoral Augment; Item Numbers: (1) 880-300/11 (Sz. 0 - cemented sm), (2) 880-300/21 (Sz. 0 - cemented lg), (3)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-01 Software Version: All software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2025
BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: TA-06-0001 Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conavi Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2025
CFS CROMER FOOD SERVICES, INC. Anderson, SC 29621 CHICKEN SALAD On White NET WT. 4.3 OZ CONTAINS: EGGS, WHEAT, SOY UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cromer Food Services, Inc.
FDA (openFDA food enforcement)
Reported Apr 30, 2025
InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
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.