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. 2,785 recalls have been distributed to Georgia in the last 12 months.
Showing 13901–13920 of 29,505 recalls
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: Battery short-run times and unanticipated stoppage may be due to user not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....
The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....
The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by...
The Issue: Device vented gas below the stated pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STANLEY Healthcare Arial 54315 Network Manager Recalled by Stanley Security...
The Issue: STANLEY Healthcare has received reports of outages on the Arial nurse call...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advincula Delineator with Ultem Plastic Soft Cup size 3.0 cm Recalled by...
The Issue: The soft, flexible cup of the Advincula Delineator may be unvalidated and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advincula Delineator with Ultem Plastic Soft Cup size 2.5 cm Recalled by...
The Issue: The soft, flexible cup of the Advincula Delineator may be unvalidated and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250) Recalled by Beckman...
The Issue: The firm has identified that cross-reactivity testing may not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.