Recalls in Georgia (page 36)
4046 recalls.
- Airova Recalls Aroeve Air Purifiers Due to Fire and Burn Hazards
Consumer productReported February 12, 2026 · The air purifiers can overheat and ignite, posing fire and burn hazards to consumers. - GLUTEN FREE 14" SEASONED VEGAN PIZZA CRUST recall (Rich Products Corp)
FoodClass IIReported February 11, 2026 · Product contains undeclared milk and egg - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3030... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1530... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0730 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0720 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0730 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0725 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0720 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0330 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Product Name: Single Use Sphincterotome V recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance. - Vivoo Sodium Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo Vaginal pH Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo Protein Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo pH Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Exploro Highly Sensitive Male Fertility / Sperm Concentration Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Male Fertility Sperm Test for Home Use recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - S. Typhi/Para Typhi A Antigen recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Menopause Test Cassette recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - LH One Step Ovulation Test Device recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - LotFancy Urinary Tract Infection Urine recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Swiss Chocolate Cake Mix recall (B.C. Williams Bakery Service, Inc)
FoodClass IReported February 11, 2026 · Undeclared Milk Allergen - Bread and Roll Mix recall (B.C. Williams Bakery Service, Inc)
FoodClass IReported February 11, 2026 · Undeclared Milk Allergen - Spice Cake Mix recall (B.C. Williams Bakery Service, Inc)
FoodClass IReported February 11, 2026 · Undeclared Milk Allergen - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Sea Moss Gel Superfood recall (Diva Fam Inc)
FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination - Lost and Found Energy recall (Fazt & Loud LLC)
FoodClass IIIReported February 11, 2026 · Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of... - Diclofenac Sodium recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported February 11, 2026 · Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%. - Trazodone Hydrochloride recall (Granules Pharmaceuticals Inc.)
DrugClass IIReported February 11, 2026 · Presence of Foreign Tablets/Capsules - Bisoprolol Fumarate and Hydrochlorothiazide tablets recall (Unichem Pharmaceuticals USA Inc.)
DrugClass IIReported February 11, 2026 · cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits. - Brand Name: Molift Product Name: Molift 4-point sling bars recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift 2-point sling bars recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number: 81559 ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number:... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number: 81557 ... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model/Catalog... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number:... recall (Fujirebio Diagnostics, Inc.)
Medical deviceClass IIReported February 11, 2026 · Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low... - Bubble Sensor for 3/8" x 3/32" tubing recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported February 11, 2026 · Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending... - FDR Visionary Suite recall (FUJIFILM Healthcare Americas Corporation)
Medical deviceClass IIReported February 11, 2026 · It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might... - Vortex Surgical Lindsell Sutured IOL Marker recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical 25GA Backflush recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical TID Pharos Illuminated Depressor recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · XXX - Rumex Disposable Diamond Dusted ILM Elevator recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical I2 Injection Kit recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Tecfen Retractable Membrane Polisher recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical 25GA I.D.D. Internal Delivery Device recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - 25GA Subretinal Injection Cannula VS0220.25 recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive VS0740.23 ... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Focalyx Fusion recall (Focalyx Technologies, LLC.)
Medical deviceClass IIReported February 11, 2026 · Software device that is an accessory for image-guided interventional and diagnostic procedures involving prostate has accessories that may not function... - NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE recall (Tornier, Inc)
Medical deviceClass IIReported February 11, 2026 · A specific lot of screws is incorrectly labeled. Screws are labeled as 5.0mmx18mm but actual screws are 5.00mmx14mm. If mismatch is detected during surgery... - VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B recall (Biomerieux Inc)
Medical deviceClass IIReported February 11, 2026 · Potential risk of Quality Control failures and/or false resistant antibiotic results when testing isolates of Enterobacterales/Enterobacteriaceae species... - CellMek SPS Sample Preparation System recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported February 11, 2026 · Sample preparation system designed to automate staining, lysing, cell washing has a software error that causes samples to be dispensed close to or touching... - PRISMAFLEX TPE2000 SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - PRISMAFLEX HF1000 SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.