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. 2,145 recalls have been distributed to Indiana in the last 12 months.
Showing 4361–4380 of 29,228 recalls
Recalled Item: Medline medical procedure kits labeled as follows: a) AAA CDS Recalled by...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) TURNOVER KIT Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) BASIC NEURO Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Patient Information Center (PIC) iX Uninterruptable Power Supply...
The Issue: Possible failure of Uninterruptable Power Supply (UPS) devices supporting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Redux Electrolyte Creme Recalled by Parker Laboratories, Inc. Due to Product...
The Issue: Product demonstrates low viscosity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models:...
The Issue: Coolant level in the cooling circuit drops below a certain level, this may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Surgical Tape Recalled by 3M Company - Health Care Business Due...
The Issue: Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr¿ger Perseus A500 Anesthesia Workstation Recalled by Draeger Medical, Inc....
The Issue: Unexpected shutdown while operating on battery power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion Pump Recalled by Baxter Healthcare Corporation...
The Issue: One device was improperly performed testing prior to release from a Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to The Alinity m...
The Issue: The Alinity m System camera detects whether tubes are "capped." If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24K Premium Lense Recalled by Ontact Inc Due to Contact lenses recalled due...
The Issue: Contact lenses recalled due to potential bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.