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Recalls distributed in Georgia

These notices name Georgia in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

5,116 stored notices name Georgia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Georgia too — those are in the archive.

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Ingenia 3.0T and 3.0T CX; Model number (REF): 1. 781342 (3.0T), 2. 781377 (3.0T), 3. 782103 (3.0T), 4. 781271 (3.0T…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 7, 2026Updated Oct 13, 2026

Salata Salad Kitchen Jalapen¿o Avocado Dressing. Keep Refrigerated. Packaged in the following sizes: 1. 12.5 fl. oz.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Salata Dressings, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Atellica CH Revised C-Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Volcano Corp.

FDA (openFDA device enforcement)

Meat & poultry

Reported Oct 6, 2026Updated Oct 25, 2026

FSIS Issues Public Health Alert for Ineligible Chicken Vienna-Style Sausage Products Illegally Imported From Jamaica

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Fsis

USDA FSIS

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton, Dickinson and Company

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Red Blood Cells, Leukocytes Reduced

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Blood Assurance Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M001314011 IMAGER II/5/ST/100/038 BX5;…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 15, 2026

INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing component. 5 units per box. Model…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CooperSurgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Criticare Technologies, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 17, 2026

Apheresis Platelets, Leukocytes Reduced, Pathogen Reduced

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

LifeSouth Community Blood Centers, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T Initial system; Model Numbers (REF): 1. 781196 (Achieva 1.5T),…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Food

Reported Sep 30, 2026Updated Oct 7, 2026

Reese's Crunchy Peanut Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Unilever North America Supply Chain Company, LLC

FDA (weekly enforcement report)

Meat & poultry

Reported Sep 25, 2026Updated Oct 25, 2026

Sempio Food Services Inc. Recalls Ready-To-Eat Chicken Stew Products Imported Without the Benefit of Import Reinspection

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sempio Food Services Inc.

USDA FSIS

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bard Access Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS: WHOLE GRAIN OATS, MILK, MARGARINE***WATER, SALT, CONTAINS LESS…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Best Friends Bakery, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo Samples Quantity 100

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

embecta Medical II LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Happiest Baby, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Plum administration sets

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Consumer products

Reported Sep 23, 2026

Intercon Foaming Pear Hand Soap With Aloe, 28.7 fl. oz., Manufactured for: Intercon Chemical Company 1100 Central…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intercon Chemical Co.

5 more products in this recall

FDA (weekly enforcement report)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.