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. 2,643 recalls have been distributed to Georgia in the last 12 months.
Showing 27421–27440 of 29,505 recalls
Recalled Item: Software correction applies to customers who use the RT Therapist Recalled...
The Issue: Software update to fix multiple safety related issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848...
The Issue: An LPC Fine Mesh Cassette failed to stay closed during processing operations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling
The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
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.
Recalled Item: VITROS Immunodiagnostic Products CK-MB Calibrators Recalled by...
The Issue: Internal testing demonstrated that opened-reconstituted VITROS CK-MB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOSHIBA Kalare Diagnostic X-Ray System K110785 Recalled by Toshiba American...
The Issue: Firm initiated recall because when radiographic conditions with the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
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.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
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.
Recalled Item: Product is distributed by Zimmer (Warsaw Recalled by Synvasive Technology...
The Issue: Various reciprocating and oscillating saw blades were incorrectly labeled....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14219-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.