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. 2,730 recalls have been distributed to Georgia in the last 12 months.
Showing 17321–17340 of 29,505 recalls
Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular E 170 Analyzer: Immunoassay Chemistry Analyzer Recalled by Roche...
The Issue: Complaints have been received concerning questionable results on analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur BNP (B-type Natriuretic Peptide) Recalled by Siemens...
The Issue: In certain scenarios the ADVIA Centaur CP, XP and XPT immunoassay analyzers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....
The Issue: Package integrity failure observed during routine shift package integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...
The Issue: if the cables of the Monica IF24 System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...
The Issue: if the cables of the Monica Novii System are removed by a user, and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Camera System Recalled by Trumpf Medical Systems, Inc. Due to The radiated...
The Issue: The radiated emission from the TruVidia" Wireless Receiver is above the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 K2 Hemodialysis Machine with software version 5.40 Recalled by...
The Issue: When the recirculation ultrafiltration (UF) Goal is set to a value greater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vado Bi-Directional Steerable Sheath 8.8F Recalled by Kalila Medical Due to...
The Issue: Torn sheath liner material was detected at the proximal end of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent...
The Issue: Falsely elevated results may be obtained when using the ARCHITECT DHEA-S...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vado Steerable Sheath 8.8F Recalled by Kalila Medical Due to Torn sheath...
The Issue: Torn sheath liner material was detected at the proximal end of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with...
The Issue: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signia" Power Handle (SIGPHANDLE Recalled by Covidien LLC Due to Product...
The Issue: Product reportedly shutting down during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Re-Entry" Malecot Nephrostomy Catheter Set Recalled by Boston Scientific...
The Issue: Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.