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.

50526–50550 of 83459

HighFDA (Devices)·Z-1261-2017·2017-03-08
Windstone Medical Arthroscopy Packs Recalled for Sterility Compromise
Windstone Medical Packaging is recalling 1,081 arthroscopy kits because the disposable gloves inside may have splits or holes that compromise sterility.
Product
Arthroscopy Pack, part number AMS2938 Arthroscopy Pack, part number AMS3639 Arthroscopy Pack, part number AMS4765 Arthroscopy Pack, part number PSS1799 Arthroscopy Pack, part number PSS1845(A
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1305-2017·2017-03-08
Windstone Medical Packaging Recalls General Packs with Defective Gloves
Windstone Medical Packaging is recalling 1,501 General Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General Pack, part number AMS5341 General Pack, part number AMS5694
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1265-2017·2017-03-08
Windstone Medical Packaging Recalls Basic Face Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 965 Basic Face Kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Basic Face Kit, part number PS517A(D
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1390-2017·2017-03-08
Cook Inc. Recalls Flexor Radial Access Sets Due to Blood Loss Reports
Cook Inc. is recalling 41,975 Flexor Radial Access Sets because a specific hemostatic valve design is associated with increased reports of blood loss.
Product
Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures
Category
Medical Device
Distribution
46 states
HighFDA (Devices)·Z-1347-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Nasal Pack, part number PSS2186
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1375-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Sterility Compromise in Knee Kits
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Total Knee Pack (15710), part number AMS6563
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1309-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits are recalled because splits or holes may compromise sterility.
Product
GYN Lap Pack, part number PSS2194(B
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1317-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in AMS kits are recalled because splits or holes may compromise sterility.
Product
HSG Pack, part number PSS3287
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1298-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Eye Plastic Tray, part number PSS1931(A
Category
Medical Device
Distribution
26 states
HighFDA (Food)·F-1546-2017·2017-03-08
Bell Stone Toffee Recalls Chocolate Products Due to Undeclared Milk Allergen
Bell Stone Toffee is voluntarily recalling specific lots of toffee products because the labels failed to identify milk as an ingredient, despite declaring butter.
Product
Dark Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-1323-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Laminectomy Pack, part number PSS1844(B
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1339-2017·2017-03-08
Windstone Medical Recalls Major Laparotomy Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 32 Major Laparotomy Packs because the disposable gloves included may have splits or holes that compromise sterility.
Product
Major Laparotomy Pack - NS, part number AMS4347
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1278-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Breast Recon Pack, part number AMS5698 Breast Recon Pack, part number AMS5698(A
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1351-2017·2017-03-08
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES Recalled for Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Product
Open Procedure Pack II, part number RMS1740(A
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1361-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Plastic Pack, part number PSS2462 Plastic Pack, part number PSS3319 Plastic Pack, part number PSS3319(A
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1385-2017·2017-03-08
Merge Healthcare Recalls Unity PACS Software Due to Image Error
Merge Healthcare is recalling Unity PACS software versions 11.0 and 11.0.1 because the software fails to add the correct tomo image.
Product
DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1373-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Total Hip Pack, part number PSS2956
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1386-2017·2017-03-08
Maquet CARDIOSAVE IABP Li-Ion Battery Recall Due to Venting Risk
Maquet is recalling Li-Ion batteries for CARDIOSAVE IABP devices after reports of venting when dropped.
Product
CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part number is 0146-00-0097 Product Usage: The CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1283-2017·2017-03-08
FDA Recalls Custom Breast Augmentation Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 229 Custom Breast Augmentation Packs because the included gloves may have splits or holes that compromise sterility.
Product
Custom Breast Augmentation Pack, part number PSS2455(D
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1349-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Ocular Plastic Pack, part number AMS3868(A
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1253-2017·2017-03-08
Phadia Recalls EliA Sample Diluent Due to Liquid Level Detection Issues
Phadia US Inc is recalling EliA Sample Diluent because liquid level detection problems in Phadia 250 instruments caused erroneous test results.
Product
EliA Sample Diluent, Article number, 83-1023-01
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1381-2017·2017-03-08
Medtronic Gloves in Custom Kits Recalled for Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Product
Vein Tray, part number AMS6312
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1268-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Sterility Compromise in Custom Kits
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Product
Basic Pack (1185), part number AMS6560
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1371-2017·2017-03-08
Medtronic Cover Light Handle Gloves Recalled for Sterility Compromise
Medtronic Cover Light Handle Disposable Gloves in AMS kits are recalled because splits or holes may compromise sterility.
Product
Stem Pack, part number AMS5166
Category
Medical Device
Distribution
26 states
HighFDA (Devices)·Z-1353-2017·2017-03-08
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom kits are recalled because splits or holes may compromise sterility.
Product
Orbitofacial Pack, part number AMS5850(A
Category
Medical Device
Distribution
26 states