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. 2,456 recalls have been distributed to Indiana in the last 12 months.
Showing 44221–44240 of 53,528 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...
The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan T 5K Motor Product Usage: Low-speed motor is used Recalled by Dental...
The Issue: The housing of 5K motor was laser marked incorrectly as a 20K motor. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...
The Issue: Failed Dissolution Specifications: Stability results found the product did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captomer-250 [succinic acid (from 250 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captomer [succinic acid (from 100 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WaterLase iPlus Dental Laser System Recalled by Biolase Technology Inc Due...
The Issue: Biolase is recalling the WaterLase iPlus Dental Laser System because of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P...
The Issue: A small number of sealed foil pouches containing the electrodes were found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...
The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...
The Issue: Two lots of screws were commingled. Screws with etching and machining for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red...
The Issue: Oregon Freeze Dry, Inc. is voluntarily recalling Mountain House Scrambled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka...
The Issue: Loosened monitor arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE Recalled by GE Healthcare, LLC...
The Issue: Failure of the CO2 detector in Single-width Airway and Extension modules,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritium Sternal Plate System Recalled by PIONEER SURGICAL TECHNOLOGY, INC....
The Issue: Lack of Sterility Assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific VersaTREK REDOX 1 Recalled by Remel Inc Due to Bottles did...
The Issue: Bottles did not provide positive signals within the time frame of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ LED Battery Charger Recalled by Integra LifeSciences Corp. Due to...
The Issue: LED battery chargers may prematurely fail and will not charge the LED...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenor is a mobile passive lift Recalled by ARJOHUNTLEIGH POLSKA SP. ZO.O....
The Issue: ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.