Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,791 recalls have been distributed to Indiana in the last 12 months.
Showing 41341–41360 of 53,528 recalls
Recalled Item: BIEST TD 80/20 (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.
Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (yellow) / 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: BIEST TD 80/20 (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.
Recalled Item: BIEST TD 86/14 (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.
Recalled Item: ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 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 80/20 (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.
Recalled Item: BIEST TD 80/20 (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.
Recalled Item: ESTRIOL (E3) : PROGESTERONE W/V (weight/volume) 4.0 : 100 MG/ML Recalled by...
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 80/20 (Estradiol USP Micronized (E2)/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.
Recalled Item: BIEST TD 80/20 (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.
Recalled Item: ESTRIOL (E3) 4.0MG capsules Recalled by the Compounder Due to 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 67/33 (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.
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: 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: Brand Name: Persona¿ Anterior Sizer with Locking Boom The Recalled by...
The Issue: Zimmer, Inc is voluntarily recalling 22 lots of Persona¿ Anterior Sizer with...
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: 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: 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: 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) 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.