State

Georgia product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43976–44000 of 83444

HighFDA (Devices)·Z-1738-2018·2018-05-16
Zimmer Biomet Recalls Gentle Threads Interference Screws Due to Sterilization Issue
Zimmer Biomet is recalling 54 Gentle Threads interference screws because overexposure to ethylene oxide sterilization may compromise the sterile barrier, potentially leading to infection.
Product
Gentle Threads, Interference Screw; Model No. 905608, for soft tissue reattachment procedures in the ankle/foot and knee.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1736-2018·2018-05-16
Zimmer Biomet Recalls Gentle Threads Interference Screws Due to Sterilization Issues
Zimmer Biomet is recalling 53 Gentle Threads Interference Screws because overexposure to ethylene oxide sterilization may have compromised the sterile barrier, potentially leading to infection.
Product
Gentle Threads, Interference Screw; Model No. 905605, for soft tissue reattachment procedures in the ankle/foot and knee.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1624-2018·2018-05-16
Boston Scientific Recalls Pinnacle Anterior Apical Pelvic Floor Repair Kits
Boston Scientific is voluntarily recalling 34 Pinnacle Anterior Apical pelvic floor repair kits due to a Class II safety concern. The devices were distributed worldwide.
Product
PFR Kit- Pinnacle, Anterior Apical; Model #M0068317100. Indicated for tissue reinforcement in women with pelvic organ prolapse.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1683-2018·2018-05-16
Siemens Recalls IMMULITE Assays Due to Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling specific IMMULITE assay lots because the instructions fail to list biotin interference concentrations, potentially causing inaccurate test results.
Product
IMMULITE 2000/IMMULITE ¿ 2000 XPi OM-MA (CA125)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1397-2018·2018-05-16
Sugarfina Platinum Bling Ring Recalled for Undeclared Fish Allergen
Sugarfina LLC is recalling Platinum Bling Rings because an internal audit found undeclared fish gelatin. The product was distributed in 16 states.
Product
Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC: 840278116139 Net W. 21g ().7 oz.) Sculpted from dark chocolate, these interlocking rings have a thin sugar shell brushed with edible silver: Ingredients: Dark Chocolate (cocoa, sugar, cocoa butter, soy lecithin…
Category
Food
Distribution
16 states
HighFDA (Devices)·Z-1617-2018·2018-05-16
Boston Scientific Recalls Capio SLIM Box 5 Sutures Due to Breakage Risk
Boston Scientific is recalling 60,538 units of Capio SLIM Box 5 sutures because they may break or detach during open surgery.
Product
Capio SLIM Box 5, Model #M0068318261; Intended for use in general suturing applications during open surgery to assist in the placement of suture material in tissues at the operative site.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1697-2018·2018-05-16
Straumann Emdogain Recalled for Unverified Raw Material Shelf Life Change
Straumann Manufacturing is recalling Emdogain multipacks because a raw material shelf-life change was implemented without submitting data to demonstrate continued product efficacy.
Product
Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article Number 075.115
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1633-2018·2018-05-16
Vygon Recalls PICC Insertion Kits Due to Sterility Risk
Vygon U.S.A. is recalling 16,520 PICC Kit units (Product Code AMS-7063-1) because potential friction holes may compromise product sterility.
Product
PICC Kit, Product Code: AMS-7063-1 Convenience kit for the insertion of PICCs into the vascular system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1754-2018·2018-05-16
Cook Inc. Recalls Connecting Tubes Due to Potential Leakage
Cook Inc. is recalling 304 connecting tubes because the cap-adapter assembly may not tighten adequately, potentially causing fluid leakage or air aspiration.
Product
Connecting Tube - Female to Male Luer Lock, HPCT8.8-80-M-FM Product Usage: The connecting tube is intended to be a conduit between a fluid reservoir and a vascular catheter in the patient. The connecting tube may be used during angiographic procedures to connect radiographic…
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-1777-2018·2018-05-16
Parker Laboratories Recalls Sterile Ultrasound Gel for Potential Seal Leaks
Parker Laboratories, Inc. is recalling Sterile Aquasonic 100 Ultrasound Transmission Gel because the packet seals may leak.
Product
Sterile Aquasonic 100 Ultrasound Transmission Gel, 20 grams, Model Number 01-01-4, 400 packets/case
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-1670-2018·2018-05-16
Siemens Dimension Sirolimus Reagent Cartridge Recalled for Biotin Interference
Siemens Healthcare Diagnostics is recalling Dimension Sirolimus reagent cartridges because biotin can interfere with test results, potentially affecting patient care.
Product
Dimension¿ Sirolimus (SIRO) Flex¿ reagent cartridge
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1669-2018·2018-05-16
Siemens Dimension Free Thyroxine Reagent Cartridge Recall for Labeling Error
Siemens is recalling Dimension Free Thyroxine reagent cartridges because the instructions for use incorrectly state the level at which biotin does not interfere.
Product
Dimension¿ Free Thyroxine (FT4L) Flex¿ reagent cartridge
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1668-2018·2018-05-16
Siemens Recalls Dimension TSHL Reagent Cartridges Due to Biotin Labeling Error
Siemens Healthcare Diagnostics is recalling Dimension TSHL reagent cartridges because the instructions for use incorrectly state the biotin concentration level at which interference does not occur.
Product
Dimension¿ Thyroid Stimulating Hormone (TSHL) Flex¿ reagent cartridge
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1765-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Patient ID Card Instructions
Bard Peripheral Vascular Inc is recalling 383 units of POWERPORT ClearVUE Slim catheters because the packaged Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1678301
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1801-2018·2018-05-16
Beaver-Visitec Recalls Hemostatic Eraser Bipolar Due to Incorrect Labeling
Beaver-Visitec International Inc. is recalling 1,025 units of Wet-Field Hemostatic Eraser Bipolar 25G instruments because they were packaged with incorrect labeling.
Product
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1402-2018·2018-05-16
Peaceful Mountain Nasal Rescue Recalled as Unapproved New Drug
Grato Holdings is recalling Peaceful Mountain Nasal Rescue dietary supplements because they are unapproved new drugs based on disease claims.
Product
Peaceful Mountain, Nasal Rescue, Dietary Supplement, Natural Sinus Support, Dist. by Peaceful Mountain, Inc. Woodbine, IA 51579
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1759-2018·2018-05-16
Synthes Sciatic Nerve Retractor Recalled for Potential Microspore Formation
Synthes (USA) Products LLC is recalling 196 Sciatic Nerve Retractors due to a potential for microspores to form on the hollow handle, which could allow fluid entry.
Product
Retractor f/Sciatic Nerve Long; Part number: 03.100.014; UDI: 10886982070630
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1772-2018·2018-05-16
Bard POWERPORT ClearVUE Implantable Port Recall for Incorrect Instructions
Bard Peripheral Vascular Inc is recalling 15 units of POWERPORT ClearVUE isp Implantable Port kits because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1689-2018·2018-05-16
Siemens ADVIA Centaur Folate Recalled for Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Folate assays because biotin interference levels are not listed in the instructions, potentially affecting test accuracy.
Product
ADVIA Centaur¿ Folate (FOL)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1778-2018·2018-05-16
Siemens Syngo.Via Software Recall for Report Functionality Defect
Siemens Medical Solutions is recalling Syngo.Via VB20A software because corrected report values are not saved or transmitted, causing the system to use original values.
Product
Syngo.Via VB20A model 1049610
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1768-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Flushing Instructions
Bard Peripheral Vascular Inc is recalling 3,196 units of POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter, REF 5676300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1764-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Patient Card Instructions
Bard Peripheral Vascular Inc is recalling POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1678300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1403-2018·2018-05-16
Energique Enervimin CNCR Focus Recalled as Unapproved New Drug
Grato Holdings, Inc. is recalling Energique Enervimin CNCR Focus dietary supplements because they are unapproved new drugs based on disease claims.
Product
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1676-2018·2018-05-16
Siemens IMMULITE 2000 Folic Acid Assay Recalled for Biotin Interference
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Folic Acid assays because biotin interference is not listed in the instructions for use.
Product
IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Folic Acid
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1678-2018·2018-05-16
Siemens IMMULITE CEA Assay Recalled for Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling IMMULITE CEA assays because biotin interference thresholds are not listed in the instructions, potentially affecting test accuracy.
Product
IMMULITE ¿ /IMMULITE ¿ 1000 CEA
Category
Medical Device
Distribution
Distributed nationwide