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. 1,077 recalls have been distributed to Indiana in the last 12 months.
Showing 16121–16140 of 29,228 recalls
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: The flow rate test verification was not properly executed for certain Sigma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL GC-Lect Agar Recalled by Becton Dickinson & Co. Due to A portion of...
The Issue: A portion of this lot was manufactured using Gentamicin instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...
The Issue: Label was incorrect. The label states that the volume of the retrieval bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tri-Flo Subglottic Suction System Recalled by Vyaire Medical Due to...
The Issue: Vyaire Medical has discovered potential patient safety risk with associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...
The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Shepherd' s Hook - Greenberg Recalled by Nico Corp. Due to Mislabeling
The Issue: Mislabeled hook pouch included a transport/storage label rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: Through investigation, it was determined that H12LP Trocars in scope of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a...
The Issue: There is a potential risk associated with the PEEK tip of the J-Plasma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPAP Mask Cushion Recalled by Compass Health Brands (Corporate Office) Due...
The Issue: A May 2015 design change in the cushion seal replacement part and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI system Product Usage: Hitachi MR system is Recalled by...
The Issue: The stainless steel belt which runs the length of the table underneath the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.