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. 1,122 recalls have been distributed to Georgia in the last 12 months.
Showing 12761–12780 of 29,505 recalls
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT YC-02220 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE KIT SL-05500 Recalled by Arrow International Inc Due...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow SPINAL ANESTHESIA SET ASA-25090-S Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits Recalled by Physio-Control,...
The Issue: Monitor/Defibrillator may not deliver a shock after the "Shock" button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT JH-05500 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1 Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (with ISE/without ISE) Recalled by Randox Laboratories,...
The Issue: Software version UI2550642107 for the RX Daytona + instrument released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system. Models 4.0...
The Issue: Three issues found: i) The Map ROI options in the ROI list in the Structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...
The Issue: Potential issue associated with the instrument -end of the shaft could fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...
The Issue: When using the Table Up/Down button, the system may experience Error 80,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...
The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 0 VIOLET 30" V-20 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 1 36 VIOLET GS-21 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Enzymatic Creatinine (ECRE_2) reagent Recalled by Siemens...
The Issue: There is a potential for falsely depressed creatinine results for patients...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polysorb Braided Absorbable Suture 1 36 VIOLET GS-24 Recalled by Covidien...
The Issue: There is a potential for packaging integrity issues impacting the humidity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.