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 16781–16800 of 53,623 recalls
Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE HONEY GRANOLA DIETARY SUPPLEMENT NET WT. 2LB...
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HI-TECH PHARMACEUTICALS PRECISION PROTEIN COOKIES & CREAM NET WT 2lbs...
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE STRAWBERRY MILKSHAKE DIETARY SUPPLEMENT NET...
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE SMORES DIETARY SUPPLEMENT NET WT. 2lb Recalled...
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE ORANGE CREAMSICLE DIETARY SUPPLEMENT NET WT....
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY SUPPLEMENT...
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE VANILLA ICE CREAM DIETARY SUPPLEMENT NET WT....
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ISOMORPH 28 PURE WHEY iSOLATE VANILLA MILKSHAKE DIETARY SUPPLEMENT NET WT....
The Issue: During an inspection by the FDA the firm was notified by FDA that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starwest Botanicals Item#: 209617-34 Recalled by Starwest Botanicals, Inc...
The Issue: Presence of E. coli species
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scooter Recalled by Merits Holdings Co. dba Merits Health Products, Inc. Due...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg MR Stylet Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Wheelchair Recalled by Merits Holdings Co. dba Merits Health Products,...
The Issue: Seat baseplate pin has broken in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg Laser Applicator Non-cooled Recalled by CLINICAL LASERTHERMIA...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tranberg MR Cannula Recalled by CLINICAL LASERTHERMIA SYSTEMS AB Due to...
The Issue: single use devices labeled as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DirectInject consists of a sterile dual paste system which is Recalled by...
The Issue: Inability for the user to inject the paste from the syringe into the target...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 Bedside Patient Monitor Recalled by Welch Allyn Inc Mortara...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD Recalled by Smiths Medical ASD Inc....
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.