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. 1,096 recalls have been distributed to Georgia in the last 12 months.
Showing 16501–16520 of 53,623 recalls
Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 70% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Double Chocolate Plant-Based Protein Shake Recalled by Pepsico Inc...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Vanilla Bean Plant-Based Protein Shake Recalled by Pepsico Inc Due to...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...
The Issue: No 510k for the product to be used in a natural or surgical opening to the body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" x 48" Elastic Poly Probe Cover Recalled by Exact Medical Manufacturing,...
The Issue: No 510k for the product to be used in a natural or surgical opening to the body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hays Ultrasound kit Item ID: H1000SE Recalled by Exact Medical...
The Issue: No 510k for the product to be used in a natural or surgical opening to the body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Probe Cover Recalled by Exact Medical Manufacturing, Inc. Due to No 510k for...
The Issue: No 510k for the product to be used in a natural or surgical opening to the body
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY10Y54R4 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY11B40R1 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY10J00R12 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic BB7D76R13 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY10D90R2 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 1A46R11 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY7M07R6 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB1H18R20 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8M63R4 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8R62R13 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10W65R1 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.