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. 2,577 recalls have been distributed to Indiana in the last 12 months.
Showing 21401–21420 of 53,528 recalls
Recalled Item: Stratum Foot Plating System-NL LP Screw 3.5x50mm ST Recalled by Nextremity...
The Issue: Product labeled as STRM-NL-3550ST, NL LP Screw 3.5x50mm ST, lot M1151 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit Recalled by Avanos...
The Issue: The connector piece to the PEG tube does not pass over the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit Recalled by Avanos...
The Issue: The connector piece to the PEG tube does not pass over the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas infinity central lab / cobas infinity core license-a Calculator/Data...
The Issue: Cobasinfinity laboratory solution Version 2.4.1 through Version 2.5.4 Using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...
The Issue: Walkers within the identified serial range have the potential for the front...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...
The Issue: Intermittent communication due to inconsistent crimping of connectors onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAG SCREW 3.2MM GUIDE PIN SLEEVE Recalled by Smith & Nephew, Inc. Due to LAG...
The Issue: LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...
The Issue: Software issue identified in the software versions syngo CT VB20 running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Some dental implant packages contain incorrect implants, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Recalled...
The Issue: When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...
The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Oral Solution 5mg per 5mL Recalled by...
The Issue: Presence of Foreign Substance; Fiber particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag Recalled by Gullah...
The Issue: The product ingredient statement does not list walnuts in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...
The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Cardiac Controls Catalogue Number CQ5052. Recalled by Randox...
The Issue: Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.