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. 1,003 recalls have been distributed to Georgia in the last 12 months.
Showing 42161–42180 of 53,623 recalls
Recalled Item: VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm) Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC TUBING SET Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) MOTOR MODULE Recalled by Microtek Medical Inc Due to This...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING 7/8' X 10' Recalled by Microtek Medical Inc Due to This recall is...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRAL WAND W/TUBING Recalled by Microtek Medical Inc Due to This recall...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY Recalled by...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoke Evacuation Tubing Set for Coherent CPG Handpiece Recalled by Microtek...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET SYSTEM WITH BELT Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talon Grasping Device Recalled by US Endoscopy Group Inc Due to A wire...
The Issue: A wire component on the distal grasping assembly of the device became detached..
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREEDOMAIRE(R) HELMET WITH MOTOR MODULE Recalled by Microtek Medical Inc Due...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING Recalled by Microtek Medical Inc...
The Issue: This recall is being conducted because a cohesive band used to package the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ergoloid Mesylates Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: during long-term stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70 Recalled by Ultra...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis confirmed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST CP 76/24: DHEA (Estriol USP Micronized (E3)/Estradiol (E2) Trit...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 91/9 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST 80/20 : PROGEST : DHEA : TESTOST (Estriol USP Recalled by the...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Domperidone BP Recalled by Freedom Pharmaceuticals Inc Due to Penicillin...
The Issue: Penicillin Cross Contamination: Potential for products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRIEST 80/10/10 (E1/E2 Trit - Estrone (E1)/Estradiol (E2) / Estriol Recalled...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 89/11 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.