State

Georgia product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54876–54900 of 83462

HighFDA (Devices)·Z-2105-2016·2016-07-06
Medical Depot Recalls Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail.
Product
Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2103-2016·2016-07-06
Medical Depot Universal Aluminum Crutches Recalled for Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of Universal aluminum crutches because the bottom metal tips may fail.
Product
Universal aluminum crutch, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2102-2016·2016-07-06
Medical Depot Recalls EZ Adjust Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of EZ adjust aluminum crutches because the tip may fail, posing a risk of injury.
Product
EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V510000·2016-07-06
MCI Recalls 2015-2016 J4500 Buses Due to Window Hardware Defect
Motor Coach Industries is recalling 2015-2016 J4500 buses because improperly installed window hardware may allow windows to open unexpectedly, increasing ejection risk.
Product
MCI — MCI J4500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2059-2016·2016-07-06
Hospira Recalls LifeShield IV Administration Sets Due to Fluid Leakage
Hospira is recalling specific LifeShield IV administration sets because intravenous fluid may leak at the CLAVE secondary port.
Product
*** 1) Product labeled in part: 14951-48; LIFESHIELD; PLUMSET WITH CONVERTIBLE PIERCING PIN, TWO INTEGRAL CLAVE PORTS AND CLAVE ON SECONDARY PORT; NOMINAL LENGTH: 104 IN (264 CM); PRIMING VOLUME: 19 ML; *** 2) Product labeled in part: 14952-01; LIFESHIELD; HEMA Y-TYPE BLOOD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2061-2016·2016-07-06
Hospira Recalls IV Administration Sets Due to Fluid Leakage Risk
Hospira is recalling specific lots of Lifeshield IV administration sets because intravenous fluid may leak at the secondary port.
Product
*** 1) Product labeled in part: 19734-28; LIFESHIELD; LIFESHIELD LATEX-FREE PLUM SET, MICRODRIP,PP SOLUSET,FILTER, 3 CLAVE PORTS, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 124 IN (315 IN); PRIMING VOLUME: 14 ML; *** 2) Product labeled in part: 19732-28; LIFESHIELD; LIFESHIELD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2093-2016·2016-07-06
Smith & Nephew Legion HK Femoral Assembly Recalled for Surface Defect
Smith & Nephew is recalling 16 units of the Legion HK Femoral Assembly because the internal surface where cement is applied is below specification.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 4 RIGHT, A/P 58.5 MM, M/L 66 MM, REF 71421364 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2058-2016·2016-07-06
Hospira Recalls PlumSet IV Administration Sets Due to Fluid Leakage
Hospira is recalling specific PlumSet IV administration sets because intravenous fluid may leak at the CLAVE secondary port.
Product
*** 1) Product labeled in part: List No. 14212-28; LIFESHIELD; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 Inch, Non-DEHP; *** 2) Product labeled in part: List No. 14254-28; LIFESHIELD; PRIMARY PLUMSET; CLAVE Port 2 CLAVE Y-Sites, 0.2 Micron Filter, 112…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2101-2016·2016-07-06
Medical Depot Recalls Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of aluminum crutches nationwide because the metal tip may fail. Users should stop using the product.
Product
Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, adult, 8 pairs per case, 3) Aluminum crutch, youth, 1 pair per case, 4) Aluminum crutch 8 pairs per case, 5) Aluminum crutch, tall adult, 1 pair per case & 6) Aluminum…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2106-2016·2016-07-06
Medical Depot Aluminum Crutches Recalled Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of Direct Supply aluminum crutches because the metal tips may fail.
Product
Direct Supply aluminum crutch, adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16212·2016-07-06
Boscov's Recalls Orbit Hoverboards Due to Fire and Explosion Hazard
Boscov's is recalling Orbit brand self-balancing scooters because their lithium-ion batteries can overheat, posing a risk of fire or explosion.
Product
Self-balancing scooters/hoverboards
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2055-2016·2016-07-06
Hospira Symbiq Infusion Pumps Recalled for Frequent False Occlusion Alarms
Hospira is recalling Symbiq One Channel Infusers due to frequent false proximal occlusion alarms that may delay or interrupt patient therapy.
Product
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2090-2016·2016-07-06
Smith & Nephew Recalls Legion HK Femoral Assemblies for Surface Defect
Smith & Nephew is recalling 12 units of Legion HK Femoral Assemblies because the internal surface is below specification, potentially affecting cement adhesion.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 3 LEFT, A/P 54.5 MM, M/L 62 MM, REF 71421373 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2094-2016·2016-07-06
Smith & Nephew Legion HK Femoral Assembly Recalled for Surface Defect
Smith & Nephew is recalling 10 units of Legion HK Femoral Assemblies because the internal cement surface is below specification.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 5 LEFT, A/P 62 MM, M/L 70 MM, REF 71421375 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1060-2016·2016-07-06
Actavis Recalls Ciprofloxacin Ophthalmic Solution Due to Impurity
Actavis Pharma Inc. is voluntarily recalling Ciprofloxacin Ophthalmic Solution due to out-of-specification results for an unknown impurity near expiration.
Product
Ciprofloxacin Ophthalmic Solution (0.3% as base), Sterile, Rx only, a) 2.5 mL Bottle, b) 5 mL Bottle, c) 10 mL Bottle, For Topical Ophthalmic Use Only, Hi-Tech Pharmacal Co. Inc., Amityville, NY 11701, NDC: a) 50383-0282-02, b) 50383-282-05, c) 50383-0282-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2099-2016·2016-07-06
Dako HER2 CISH pharmDx Kit Recalled for Incorrect Probe Concentration
Dako North America Inc. is recalling 31 kits of the HER2 CISH pharmDx Kit because the HER2 probe concentration was too low.
Product
Dako HER2 CISH pharmDx Kit, product code: SK 109 Product Usage: For in vitro diagnostic use. HER2 CISH pharmDx Kit is intended for dualcolor chromogenic visualization of signals achieved with directly labeled in situ hybridization probes targeting the HER2 gene and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2118-2016·2016-07-06
Philips Ingenuity Core 128 CT Scanner Recalled for Image Artifacts
Philips is recalling 19 Ingenuity Core 128 CT scanners because software version 3.5.4 may cause swirl-like artifacts on images, potentially requiring patient rescans.
Product
Ingenuity Core 128-Computed Tomography X-ray system Product Usage: The Ingenuity Core 128 scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2095-2016·2016-07-06
Smith & Nephew Legion HK Femoral Assembly Recalled for Surface Defect
Smith & Nephew is recalling 97 units of the Legion HK Femoral Assembly because the internal surface is below specification, potentially affecting cement adhesion.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 5 RIGHT, A/P 62 MM, M/L 70 MM, REF 71421365 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2057-2016·2016-07-06
Dynarex Recalls Specimen Containers Due to Incorrect Sterile Labeling
Dynarex Corporation is recalling non-sterile specimen containers that were mistakenly packed in cartons labeled as sterile. The recall covers specific lots distributed in the US and Canada.
Product
dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product Usage:containers for sample collection
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2091-2016·2016-07-06
Smith & Nephew Recalls Legion Hinge Knee Femoral Assemblies
Smith & Nephew is recalling Legion Hinge Knee femoral assemblies because the cement application surface is below specification.
Product
LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 3 RIGHT, A/P 54.5 MM, M/L 62 MM, REF 71421363 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2117-2016·2016-07-06
Philips Ingenuity Core CT Systems Recalled for Image Artifacts
Philips is recalling 18 Ingenuity Core CT systems because software version 3.5.4 may cause swirl-like artifacts on images, potentially requiring patient rescans.
Product
Ingenuity Core-Computed Tomography X-ray system Product Usage: The Ingenuity Core scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2084-2016·2016-07-06
Integra LifeSciences Recalls METASURG Capture Screw System K-wires
Integra LifeSciences is recalling 182 K-wires used in the METASURG Capture Screw System because they do not meet material, surface, and dimensional specifications.
Product
K-wire, Smooth Double-pointed 0.8 x 90mm, a component of the METASURG Capture Screw System The K-wire is used in conjunction with the 2.0 mm cannulated screws for the METASURG Capture Screw System. The K-wire is used by the physician to insert into the bone and to act as a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2116-2016·2016-07-06
Philips Brilliance 64 CT Scanner Recall for Image Artifacts
Philips is recalling 94 Brilliance 64 CT scanners due to intermittent swirl-like ring artifacts on images, which may require patient rescans.
Product
Brilliance 64, Computed Tomography X-ray system Product Usage: The Brilliance CT 64 scanner is a whole body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1052-2016·2016-07-06
Lupin Recalls Lisinopril and Hydrochlorothiazide Tablets Due to CGMP Deviations
Lupin Pharmaceuticals is recalling specific lots of Lisinopril and Hydrochlorothiazide tablets because they were manufactured using active ingredients that failed specifications.
Product
LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1053-2016·2016-07-06
Aloe Source Recalls Topical Analgesic Products Due to Manufacturing Deviations
The Aloe Source is voluntarily recalling specific lots of aloe SPORT liniment and eucalyptus cream due to CGMP deviations.
Product
aloe SPORT liniment TOPICAL ANALGESIC 8 fl oz. tube, ALOE VERA Liniment Topical Analgesic 8 fl oz. bottle, Manufactured by Coats International, Inc., the ALOE SOURCE SPORT Sport Thermogenic Eucalyptus Cream 1 fl oz. plastic bottle, Dallas, TX 75243, NDC 58826-704-08, UPC…
Category
Drug
Distribution
Distributed nationwide