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. 2,696 recalls have been distributed to Indiana in the last 12 months.
Showing 11481–11500 of 13,412 recalls
Recalled Item: Vitamin C (ascorbic acid) Injection Recalled by Flawless Beauty LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saluta (reduced glutathione) Powder for Injection Recalled by Flawless...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Flawless Beauty LLC Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotidine Injection 20 mg Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Baxter Healthcare Corporation has received a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...
The Issue: Defective Delivery System; defective valve
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Cross Contamination with Other Products: Four lots of Liothyronine Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Nylon fibers found in a bottle of 0.9%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Midazolam HCl 1 mg/ml in 0.9% Sodium Chloride in 50 mL and 100 mL IV bag...
The Issue: Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate 0.2 mg/ml Recalled by Pharmakon Pharmaceuticals Due to...
The Issue: Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atropine Sulfate 0.4 mg/ml Injection Recalled by Pharmakon Pharmaceuticals...
The Issue: Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Midazolam HCl 2 mg/ml in 0.9% Sodium Chloride in 30 mL PVC Vial Recalled by...
The Issue: Incorrect/ Undeclared Excipient: Contains undeclared benzyl alcohol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Orally Disintegrating Tablets 5 mg Recalled by Apotex Corp. Due...
The Issue: Subpotent Drug: Out of specification (OOS) results at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.