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. 1,781 recalls have been distributed to Indiana in the last 12 months.
Showing 50961–50980 of 53,528 recalls
Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364M...
The Issue: When these lots of control material are reconstituted, the positive control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...
The Issue: When these lots of control material are reconstituted, the positive control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24 Fr 8mm Sft Flow Straight Wir The Sarns Aortic Recalled by Terumo...
The Issue: The presence of plastic flash was identified at the tip of certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E...
The Issue: When these lots of control material are reconstituted, the positive control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24 Fr 8mm Soft Flow Ang W/L The Sarns Aortic Recalled by Terumo...
The Issue: The presence of plastic flash was identified at the tip of certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364N...
The Issue: When these lots of control material are reconstituted, the positive control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24 Fr 8mm Sft Flow Straight The Sarns Aortic Cannula Recalled by Terumo...
The Issue: The presence of plastic flash was identified at the tip of certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Boxes labeled as CIP5 may contain cartridges of AMP5.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nalbuphine HCl Injection Recalled by Hospira, Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Complains of a loose crimp applied to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isovue -370 (Iopamidol) Injection 76% Recalled by Bracco Diagnostic Inc Due...
The Issue: Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorouracil Topical Cream USP Recalled by Taro Pharmaceuticals U.S.A., Inc....
The Issue: Product Lacks Stability: Out-of-specification (OOS) results were observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil(SCALP OIL)...
The Issue: Subpotent; 22 month stability timepoint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isovue -300 (Iopamidol) Injection 61% Prefilled Recalled by Bracco...
The Issue: Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Recalled by Hill Dermaceuticals,...
The Issue: Subpotent; 12 month stability timepoint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-322 Recalled by ConMed...
The Issue: ConMed received complaints from a user facility reporting that the WANG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-221 Recalled by ConMed...
The Issue: ConMed received complaints from a user facility reporting that the WANG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-222 Recalled by ConMed...
The Issue: ConMed received complaints from a user facility reporting that the WANG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. SW-121 Recalled by ConMed...
The Issue: ConMed received complaints from a user facility reporting that the WANG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sukhi's Gourmet Indian Food Recalled by Jagpreet Enterprises Inc. Due to A...
The Issue: A consumer complaint determined that some boxes of Red Curry and Vegetables...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...
The Issue: GE Healthcare is aware of a potential safety issue associated with the use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.