All recall categories

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.

5,046 stored notices name Georgia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Georgia too — those are in the archive.

Medical devices

Reported Jan 17, 2024

Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…

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

Bard Peripheral Vascular Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

CD11b APC: ASR, REF: 340936, and CE, REF: 333143

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Food

Reported Jan 17, 2024

Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with…

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

Eban's Bakehouse LLC

6 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 17, 2024

Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7

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

Garden Spot Foods, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2024

Incisive CT, model 728143 & 728144 running Software Version 5.0.0.

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

Philips Healthcare (Suzhou) Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010,…

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

Townsend Design

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only

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

Natus Medical Incorporated

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…

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

Philips Respironics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Alinity ci-series System Control Module, REF: 03R70-01

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an…

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

Acumed LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number…

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AcuMatch Hip System, Catalog Number 142-32-27

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

Exactech, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Injection Needle, REF: 25207

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

Karl Storz Endoscopy

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 27, 2023

Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356,…

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

Kenover Marketing Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 27, 2023

0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…

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

Nurse Assist, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting…

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Philips Allura systems with monoplane fixed ceiling mounts: 722001 Allura Xper FD10C 722003 Allura Xper FD10 722006…

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

Philips Medical Systems Nederland B.v.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 27, 2023

Cantaloupe Chunks 9oz (255g) UPC 8 26766 13923 1 & 18 oz (1 LB 2 OZ) 5??g UPC 8 26766 13917 0 Dist By Renaissance Food…

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

Renaissance Food Group

15 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 27, 2023

HMC Farms Peaches 2lb Gusset Bag

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

The HMC Group Marketing Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 20, 2023

Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157

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

E.A. Sween Co.

FDA (openFDA food enforcement)

Food

Reported Dec 20, 2023

Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection

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

Houdini Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 20, 2023

CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP)…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

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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.