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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 14441–14460 of 53,528 recalls
Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: investigation into a customer complaint...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw Recalled by Wright...
The Issue: Incorrect product is contained in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...
The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUBS Naturals Fountain of Youth Formula Recalled by Slayer Forever, LLC dba...
The Issue: Supplement contains undeclared milk from MCT oil powder ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IPELA FHD PTZ TILE KITS with Axis cameras used in Recalled by Natus...
The Issue: Tile kits that allow one to install and situate a video camera within a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vagus Nerve Stimulation (VNS) Therapy Leads Recalled by LivaNova USA, Inc....
The Issue: A manufacturing issue may cause the silicone tubing wall thickness of vagus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telmisartan and Hydrochlorothiazide Tablets Recalled by Torrent Pharma Inc....
The Issue: Superpotent; Hydrochlorothiazide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...
The Issue: The European version of the DiaTrust COVID-19 Ag Rapid Test is not approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemashield Gold Knitted Bifurcated Recalled by Maquet Cardiovascular, LLC...
The Issue: There is a probable mislabeling of product. A Hemashield Platinum Woven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic...
The Issue: ¿2 Microglobulin (B2M) Reagent Lot 211446 Bias with Quality Control and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARDY DIAGNOSTICS CatScreen Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Rotaclone Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Michels Transport Medium Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls Recalled by MEDLINE...
The Issue: Affected product was shipped from the warehouse at room temperature instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: activforce 2 package labeling: Model: Activ5-M R 201-200563 Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Recalled by ROi CPS LLC Due to Kits lacks rubber latex warning label.
The Issue: Kits lacks rubber latex warning label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.