State

Georgia product recalls

73,824 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,635
Critical: 1,471
Severe: 2,567
Most recent: 2026-11-04

Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51551–51575 of 83459

ModerateFDA (Devices)·Z-0820-2017·2016-12-28
Stanmore Tibial Component Fixed Hinge Recall Due to Pouch Puncture
Stanmore Implants Worldwide Ltd. is recalling 13 units of Tibial Component Fixed Hinge Small Long and Short due to punctured packaging.
Product
Tibial Component Fixed Hinge Small Long; Tibial Component Fixed Hinge Small Short The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the knee joint, distal femur, proximal femur or total femur bone
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0231-2017·2016-12-28
Sage Products Recalls Chlorhexidine Gluconate Cloth Due to CGMP Deviations
Sage Products LLC is recalling 2% Chlorhexidine Gluconate Cloth due to CGMP deviations and potential contamination. The product was distributed nationwide and internationally.
Product
CHLORHEXIDINE GLUCONATE — CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE GLUCONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0384-2017·2016-12-28
Teleflex Medical Recalls LMA MADgic Atomization Devices for Spray Defect
Teleflex Medical is recalling LMA MADgic atomization devices because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.
Product
LMA MADgic, Atomization Device with 3mL Syringe, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0888-2017·2016-12-28
Owens & Minor Recalls Medi Choice Arm Slings Due to Surface Contamination
Owens & Minor is voluntarily recalling specific lots of Medi Choice Arm Slings due to surface contamination identified through customer complaints.
Product
Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA, 24 ENCA ASL 2104 Medium 8 x 15 Inch 1/EA, 24 ENCA ASL 2105 Large 8.5 x 17.5 Inch 1/EA, 24 ENCA ASL 2106 Extra-Large 9 x 20 Inch 1/EA, 24 ENCA ASL 2150 Universal 7 x 18 Inch 1/EA, 24 ENCA Medical - An arm sling…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0822-2017·2016-12-28
Stanmore Implants Recalls Punctured Femoral Shaft Components
Stanmore Implants Worldwide Ltd. is recalling 11 femoral shaft components due to punctured packaging reported by customers.
Product
Femoral Shaft L=120mm; Femoral Shaft L=135mm; Femoral Shaft L=150mm The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the knee joint, distal femur, proximal femur or total femur bone
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0381-2017·2016-12-28
Teleflex Recalls LMA MADomizer Sprays Due to Inadequate Atomization
Teleflex Medical is recalling LMA MADomizer devices because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.
Product
LMA MADomizer, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce a straight stream instead of a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0385-2017·2016-12-28
Teleflex Recalls LMA MADett Endotracheal Tubes for Inadequate Anesthesia Delivery
Teleflex Medical is recalling LMA MADett endotracheal tubes because they may fail to atomize medication, potentially causing inadequate anesthesia.
Product
LMA MADett, Endotracheal tube Mucosal Atomization Device, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0386-2017·2016-12-28
Teleflex Recalls LMA MADdy Topical Anesthesia Sprays Due to Delivery Defect
Teleflex Medical is recalling LMA MADdy topical anesthesia sprays because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.
Product
LMA MADdy, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce a straight stream instead of a fully…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0882-2017·2016-12-28
Amendia Dual Stylet Needle Recall Due to Unacceptable Packaging Seals
Amendia, Inc. is recalling 1,078 Dual Stylet Needles because packaging seals are compromised by channels or voids, potentially affecting product integrity.
Product
Dual Stylet Needle, Part Number 812-11R-15 The guide wire is passed through the cannulated handle of the Dual Stylet Needles and pressed into the bone
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0383-2017·2016-12-28
Teleflex Medical Recalls Flexi Nozzle Short Sprayers for Anesthesia Delivery
Teleflex Medical is recalling Flexi Nozzle Short sprayers because they may deliver a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.
Product
FLEXI NOZZLE SHORT Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce a straight stream instead of a fully…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0872-2017·2016-12-28
Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion
Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Product
8450-010-040 4.0MM Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the attachment on…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0868-2017·2016-12-28
Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion
Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Product
8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0826-2017·2016-12-28
Medtronic Recalls Affinity Fusion Oxygenators Due to Plastic Flash Defect
Medtronic is voluntarily recalling specific lots of Affinity Fusion Oxygenators because of an out-of-specification condition involving additional plastic in the arterial sampling port.
Product
Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion Tubing Packs The Affinity Fusion Oxygenator with Integrated Arterial Filter with or without the Cardiotomy/Venous Reservoir with Balance¿1 Biosurface is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0833-2017·2016-12-28
Ben & Jerry's Brownie Batter Core Ice Cream Recalled for Plastic Pieces
Unilever is recalling Ben & Jerry's Brownie Batter Core Ice Cream because certain pints may contain soft plastic pieces.
Product
Ben & Jerrys Brownie Batter Core Ice Cream One Pint (473 mL). Case UPC- 10076840529879 Consumer UPC - 7684052987 Paper carton 8 units per shrink-wrapped case Frozen
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0823-2017·2016-12-28
Stanmore Implants Recalls Punctured Femoral Stem Components
Stanmore Implants Worldwide Ltd. is recalling 15 femoral stem components because customer inquiries reported that the device stem punctured the packaging pouch.
Product
Femoral Integral Shaft & Stem 15x27 HA Coated; Femoral Integral Shaft & Stem 15x30 HA Coated; Femoral Integral Shaft & Stem 30x27 HA Coated; Femoral Integral Shaft & Stem 30x30 HA Coated The product is a component is a systems that is intended for the replacement if…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0880-2017·2016-12-28
Stryker Recalls Kirschner Wires Due to Potential Sterile Pouch Seal Failure
Stryker Howmedica Osteonics Corp. is recalling specific lots of GAM Kirschner Wires and T2 K-Wires because a manufacturing error may have compromised the sterile pouch seal.
Product
GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 K-Wire Recon, Stryker Trauma GmbH, Prof.-Kuntscher-Strasse 1-5, Schonkirchen, Germany 24232; T2 K-Wire, Sterile R Intended for the temporary stabilization of bone segments or fragments
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0815-2017·2016-12-28
Brownwood Farms Jalapeno Cherry Salsa Recalled for Undeclared Yellow 5
Brownwood Farms is recalling Jalapeno Cherry Salsa because it contains Yellow 5, an ingredient not declared on the label.
Product
Brownwood Farms Jalapeno Cherry Salsa. 21oz glass bottles and 1 gallon. Private labels: Arbor Day Farm (Cherry Jalapeno Salsa 21oz). Kimmel Orchard & Vineyard.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0821-2017·2016-12-28
Stanmore Implants Recalls Tibial Components Due to Packaging Puncture
Stanmore Implants Worldwide Ltd. is recalling 51 tibial components because the device stem may have punctured the sterile packaging.
Product
Tibial Component Metal Cased Small Long; Tibial Component Metal Cased Small Short; Tibial Component Metal Cased Std Long; Tibial Component Metal Cased Std Short The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0382-2017·2016-12-28
Teleflex Medical Recalls Flexi Nozzle Long Sprayers for Inadequate Atomization
Teleflex Medical is recalling Flexi Nozzle Long sprayers because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.
Product
FLEXI NOZZLE LONG, 10 Boxes of 25 units each Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce a straight…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0883-2017·2016-12-28
Amendia Savannah-T Straight Rods Recalled for Packaging Seal Defects
Amendia, Inc. is recalling Savannah-T Straight Rods because some packages have unacceptable seals with compromised integrity.
Product
Savannah-T Straight Rod, 200mm, Part Number 10704-200; Savannah-T Straight Rod, 250mm, Part Number 10704-250; Savannah T-Straight Rod 300mm, Part Number 10704-300; Savannah-T Straight Rod, 400mm, Part Number 10704-400; Savannah-T Straight Rod, 500mm; Savannah-T High Top Straight…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0874-2017·2016-12-28
Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion
Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Product
8450-009-040 4.0MM Precision Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0867-2017·2016-12-28
Synthes VA Implant Rack Recalled for Incorrect Assembly
Synthes (USA) Products LLC is recalling 31 units of the VA Implant Rack for the Compact Distal Radius System because incorrect assembly could cause screws to touch the surface beneath the rack.
Product
Synthes VA Implant Rack for the Compact Distal Radius System Tray/Surgical/Instrument
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0783-2017·2016-12-28
Ultroid Mobile Generator and Sterile Probes Recalled for Quality System Failures
Ultroid Technologies is recalling 62 mobile generator units and sterile probes because they were not manufactured under required quality system controls.
Product
Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile Disposable Probes
Category
Medical Device
Distribution
34 states
ModerateFDA (Devices)·Z-0864-2017·2016-12-28
Ortho-Clinical Diagnostics Recalls VITROS CRP Slides Due to Result Bias
Ortho-Clinical Diagnostics is recalling VITROS CRP Slides because the diluent contains endogenous CRP, which can cause falsely high test results if not subtracted.
Product
VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 slides per sales unit), Catalog # 1926740 and 2) , VITROS¿ Chemistry Products CRP Slides (90 slides per sales unit), Catalog # 1926740
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0879-2017·2016-12-28
OrthoPediatrics PediNail Cortical Screw Recalled for Dimensional Discrepancy
OrthoPediatrics is recalling 22 PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screws because they measure 50mm instead of the labeled 48mm.
Product
OrthoPediatrics PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screw
Category
Medical Device
Distribution
7 states