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 48,124 notices were distributed nationwide, so they reach Georgia too — those are in the archive.
Reported Aug 5, 2015
Invivo Expression MRI Patient Monitoring System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence technology. Intended to produce cross-sectional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2015
SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP, REF 19-4137, STERILE EO, Rx only. Apply clamps parallel to the skin with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Symmetry Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
ANSPACH - Fluted Drum, Side Cut only 10MM x 14MM , REF L-10DRC-G1 Cutting shaping bone including spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
33 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
American Catheter / Cholangiogram Catheter 9100 Series.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Catheter Corp.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Polaris 4.75 TI Spinal System, 4.0 x 20 MM, Closed MAS, Closed Head Multiaxial Screw, Non-Sterile, Rx Only, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Spine, LLC
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Ring Transjugular Intrahepatic Access Set Product Usage: The Ring Transjugular Intrahepatic Access Sets are intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Usage: The CooperSurgical Milex Vaginal-Hymenal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Silhouette Lift, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Western / Scott Fetzer Company
FDA (openFDA device enforcement)
Reported Jul 23, 2015
Brown Packing Recalls Veal Products Due To Possible E. Coli Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Brown Packing
USDA FSIS
Reported Jul 22, 2015
Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 The Alere" i Influenza A & B assay, performed on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere Scarborough, Inc. dba Binax, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Diet Bubba Cola, 20 FL. OZ (1.25 PT) 591 mL INGREDIENTS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, CARAMEL COLOR,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dr. Pepper Snapple Group Inc.
FDA (openFDA food enforcement)
Reported Jul 22, 2015
MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have comfortable rounded grips for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Etac Supply Center Ab
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107. Intended to provide immobilization…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Apex ARC Hip Stem, HA Coated, Size 5; Product Code: HC-21005-HA Product Usage: The Apex ARC Hip Stem is the femoral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omnilife Science Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Sysco International Whole Segments Mandarin Oranges In Light Syrup Net Wt. 6 LB 10 OZ (3.01 kg) NDC: 074865629065; 6…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sysco Corporation
FDA (openFDA food enforcement)
Reported Jul 15, 2015
A.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a means of bone fixation and helps…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2015
Breast Pack - contains Devon Light Glove Used during surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare, LLC.
50 more products in this recall
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.