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 16081–16100 of 53,528 recalls
Recalled Item: Sterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC Due...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE PDM-Masimo SpO2. Physiological data monitor. Recalled by GE...
The Issue: Masimo SpO2 Saturation Values can become frozen after an extended length of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen Recalled by...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Galan 3T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DermOtic Oil (fluocinolone acetonide oil) 0.01% Ear Drops 20 mL bottles...
The Issue: Presence of Foreign Substance: Potential for broken glass within the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: The number of customer complaints for ripping...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: The number of customer complaints for ripping...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems Recalled...
The Issue: The high and low level "Quality Controls" demonstrate a positive bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 5Fr. pacing catheter 6 Fr....
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90. radiography and fluoroscopy system Recalled by Philips...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm Recalled by Arrow...
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr....
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm Recalled...
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.