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 15581–15600 of 29,228 recalls
Recalled Item: Affixus Hip Fracture Nail Left 125 11 mm x 320 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 130 11 mm x 380 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 13 mm x 340 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 280 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 440 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 130 11 mm x 400 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 130 11 mm x 400 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 125 11mm x 180mm Recalled by Zimmer Biomet, Inc....
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 500 Remote Control (MMT-500 Recalled by Medtronic Inc. Due to...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio MAX (model number 10762470) with Tube stand 3D V Recalled by Siemens...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio (model number 10281013 or 10281163) with Tube stand 3D Recalled by...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Multix MT (model number 8395415 or 8395399 or 8395381) Recalled by...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscopy Instruments Instructions For Use (IFU) for the following:...
The Issue: The Manual cleaning process and the usability of the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multix Fusion system is a radiographic system: Models: Multix Fusion...
The Issue: Steel cables inside the lifting column of the overhead tube, may rapture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise Imaging Desktops Enterprise Imaging Desktops (Radiology...
The Issue: Adding an additional comparison study to the Clinical Side Bar in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...
The Issue: Expiration date on the label is incorrect. Correct expiration date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module...
The Issue: A software malfunction of the infuser when used with a MedNet Custom Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.