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.
5,046 stored notices name Georgia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported Apr 1, 2020
Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diabetes Care, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
LN 3R70-01; software version 2.6.2 and earlier. The software is used with the Alinity i (LN 03R65-01) processing module…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Apr 1, 2020
1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Raisins packed in following brand names and sizes: 6 pack cartons (6 X 1 oz. boxes) - Pickwell Farms, Southern Grove,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caruthers Raisin Packing Co., Inc.
FDA (openFDA food enforcement)
Reported Apr 1, 2020
NaviCare Patient Safety Software Versions 3.5.400-3.9.300. The NaviCare Patient Safety (Patient Safety) Software is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Cardiovascular Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
RayStation standalone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 7.0, 8.0, 8.1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the determination of direct bilirubin SMN: 11097532 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skytron, Div. The KMW Group, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2020
Southern Sisters Gourmet Apple Crisp mix
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southern Sisters Gourmet
7 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 1, 2020
Whole Foods Market Green Chile Chicken Tamale served as a Family Meal, Chef's Case, Packaged, Frozen and on he hot bar…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Mar 25, 2020
Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070K NN071K NN072K…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2020
Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyers Grand Ice Cream, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 25, 2020
Medtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2020
IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and OUS: LKE21 - Product Usage: For in vitro diagnostic use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2020
Vita Wild Herring in Wine Sauce 32oz plastic jar, UPC 22635 40011, 6 jars per case Ready to Eat Keep Refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vita Food Products, Inc.
FDA (openFDA food enforcement)
Reported Mar 18, 2020
Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ARJOHUNTLEIGH POLSKA Sp. z.o.o.
FDA (openFDA device enforcement)
Reported Mar 18, 2020
Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2020
Kaiser Mild Banana Pepper Rings 1/4 KK in 1 gallon plastic bottles (4 gallons per case).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kaiser Pickles LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2020
Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535 B36004540 B36004545 B36004550 B36004555…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medicrea International
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2020
QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
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.