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. 2,747 recalls have been distributed to Indiana in the last 12 months.
Showing 5061–5080 of 29,228 recalls
Recalled Item: Ambu aView 2 A Monitor Recalled by Ambu Inc. Due to Instructions for Use...
The Issue: Instructions for Use have been updated to add the following warning: Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive SuperPulsed Laser System TFL Fiber Stripper Recalled by Olympus...
The Issue: The strippers and cleavers are provided non-sterile and labelled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLTIVE SuperPulsed Laser Fibers Recalled by Olympus Corporation of the...
The Issue: Affected products may potentially have a breached sterile pouch seal. A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive SuperPulsed Laser System TFL FIBER CLEAVER Recalled by Olympus...
The Issue: The strippers and cleavers are provided non-sterile and labelled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-V2 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-VH Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-VHR Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. BF-XP190 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-V2R Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-5R Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. BF-P190 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-5 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. ENF-XP Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for Recalled by...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.