Product Recalls in Georgia
Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,550 recalls have been distributed to Georgia in the last 12 months.
Showing 45661–45680 of 53,623 recalls
Recalled Item: Anspach Pneumatic and Electric Motor Systems. Intended for cutting and...
The Issue: Several attachments and handpieces failed to meet the expected sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACROLYTE Premie Dispersive Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed Corporation has received complaints regarding sparking, no output and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Medical Ultraview SL Command Module Recalled by Spacelabs...
The Issue: A software anomaly causes temperature alarm limits to change to limits which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Post Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Rod Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luxurian. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraslim. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Photonica Light Modulator. These include all products labeled as UltraSlim...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a potential risk when using LANTIS OIS System client software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...
The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemo-Stat Solution Recalled by Axcentria Pharmaceuticals, LLC Due to...
The Issue: Marketed without an Approved NDA/ANDA; product is being manufactured and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Philips Ingenia Recalled by Philips Medical Systems, Inc. Due to In...
The Issue: In spine clinical workflows, cross lines may be used to determine the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging It is a medical image and information Recalled by...
The Issue: The firm has identified a software issue which may cause a discrepancy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The...
The Issue: "Advocate Redi-Code + BMB-BA006A Blood Glucose test strips" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particular Matter: Potential glass delamination and consistent...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particular Matter: Potential glass delamination and consistent...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Barricini Milk Chocolate Peanut Butter Pretzels in Net Wt 6.5 oz. plastic...
The Issue: Undeclared wheat. The back panel applied to some containers of milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caravelle CHILI POWDER HOT Net Weight 8 oz. (227G) Recalled by Anhing...
The Issue: Anhing Corporation is recalling Caravelle Brand Chili Powder because it has...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alere Triage¿ D-Dimer Test PN 98100 Recalled by Alere San Diego, Inc. Due to...
The Issue: Alere initiated this recall because a limited number of Alere Triage¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kenex Radiation Shield and surgical lamps installed with GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.