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 48,132 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported Apr 1, 2015
Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouches with Tyvek header (9.5 x 13.63 x 3.75")…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ameda, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Diamondback 360 Coronary Orbital Atherectomy System, Model Number: DBEC-125. The system is indicated to facilitate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardiovascular Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.fgf brands, Inc.
FDA (openFDA food enforcement)
Reported Apr 1, 2015
GE Healthcare, SIGNA 1.5T TWINSPEED, SIGNA INFINITY MRISYSTEM, SIGNA 3.0T INFINITY WITH EXCITE, SIGNA 3.0T WITH EXCITE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by Titan Spine, LLC. Endo TCS driver is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Titan Spine, LLC
FDA (openFDA device enforcement)
Reported Mar 25, 2015
ML 7090 Calibrated LASIK Blade (CLB); CLB CALIBRATED LASIK BLADE 10. ML 7090 Calibrated LASIK Blade (CLB) is to be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med-logics Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
Puritan absorbent foam tipped applicator; Catalog Number 25-1406 1 PF BT. Sterile absorbent foam tipped applicator used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Puritan Medical Products Co., LLC
FDA (openFDA device enforcement)
Reported Mar 25, 2015
Crea A and B membranes, packaged 4 per box Used in conjunction with the ABL800 FLEX analyzers which are intended for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2015
CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical
FDA (openFDA device enforcement)
Reported Mar 25, 2015
Medstream 81" (206 cm) 20 drop Universal Administration Sets. Disposable IV infusion set with 3 year expiration date.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Infusion Inc. dba Trucare Biomedix-USA
FDA (openFDA device enforcement)
Reported Mar 18, 2015
TranSmart Raspberry Filled frozen unbaked cookie dough, 108/1.75 oz. units, CSM Bakery Products, 3301 Montreal…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CSM Bakery Products NA-Atlanta Frozen
FDA (openFDA food enforcement)
Reported Mar 18, 2015
GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pivotal Health Solutions
FDA (openFDA device enforcement)
Reported Mar 18, 2015
RAPIDPoint 405 Blood Gas Analyzer; Siemens Material Number: 10310464, 10322347, 10314817, 10317193, 10318999, 10320055,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Dr. Praeger's Sensible Foods Bombay Curry Veggie Burgers 11 oz retail box Manufactured by Dr. Praeger's Sensible Foods…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ungar's Food Products, Inc.
FDA (openFDA food enforcement)
Reported Mar 18, 2015
GROUND CUMIN STERILE TREATED PROD. OF TURKEY, 50 LBS.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wm. E. Martin & Sons Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 18, 2015
Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
SMARTSET GHV Gentamicin Bone Cement. A self-curing, radiopaque, polymethyl methacrylate based cement containing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
GROUND CUMIN SEED, 50 LBS NET, ETO STERILE TREATED
High riskUsing this product could cause serious injury, illness or death — stop using it now.Morris J. Golombeck, Inc.
FDA (openFDA food 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.