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. 960 recalls have been distributed to Indiana in the last 12 months.
Showing 47981–48000 of 53,528 recalls
Recalled Item: (Siemens Rad Fluoro Uro Systems) Ysio Recalled by Siemens Medical Solutions...
The Issue: A potential malfunction and hazard to patients exists when using the Ysio,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1650 System Software: 1) V4.01 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2400 System Software V4.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro system (Luminos dRF and Uroskop Omnia Recalled by...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1800 System Software V2.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loratadine Recalled by Novartis Consumer Health Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: The products are being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Creafuse Fruit Punch Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Creafuse Grape Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GoPicnic Black Bean Dip & Plantain Chips Recalled by GoPicnic, Inc. Due to...
The Issue: The chocolates included in the meal kits may contain undeclared milk allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DANNON OIKOS Fruit on the Bottom GREEK NONFAT YOGURT BLUEBERRY 0% FAT...
The Issue: OIKOS Nonfat Yogurt Blueberry Flavor Single Serve 5.3 oz cups were recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gopicnic Recalled by GoPicnic, Inc. Due to Undeclared Milk
The Issue: The chocolates included in the meal kits may contain undeclared milk allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Watson...
The Issue: Defective Container: Defective bottles may not have tamper evident seals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminosyn II Recalled by Hospira Inc. Due to Presence of Particulate Matter:...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg...
The Issue: Presence of Foreign Substance: This recall is being conducted due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CPT¿ Femoral Stem (CPT 12/14 STEM SIZE 0 COCR Recalled by Zimmer, Inc. Due...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versys¿ Beaded Fullcoat Femoral Stem (POR FULL-CT FEM ST 11X160MM Recalled...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: Terino Square Chin-Style II-Medium Recalled by Implantech...
The Issue: Implantech initiated a voluntary recall of certain lots of Terino Square...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Vision Mounting Arm Recalled by Stryker Endoscopy Due to When...
The Issue: When positioning the display located on top of the video cart, it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: There are artifacts appearing on the Tracker images during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.