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. 1,916 recalls have been distributed to Indiana in the last 12 months.
Showing 26721–26740 of 29,228 recalls
Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pO2 D999 membrane units. Distributed by Radiometer America Recalled by...
The Issue: RADIOMETER became aware that the regarded lot pO2 units 942-042R0971 were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System UC Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System CPS Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product...
The Issue: One of the dental implants do not have the internal hex feature. One of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595203110 Articular Surface XLPE CR ART SURF 3 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3536A Options A20 -...
The Issue: Error in the printing of the therapy energy setting labels on Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001131 Femur CR PRC SURF HDN FEM CO-NID AML Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595001201 Femur CR-FLEX PCT FEM B-L Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595201201 Femur CR-FLEX POR FEM B-L Rx Recalled by Zimmer, Inc. Due to...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00587806126 Patella MICRO POROUS PAT 26MM X 10MM Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597106126 Provisional ALL POLY PAT PROV MICRO SZ 26 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65597201333 Femur CR POR FEM SURF HDN HATCP CML Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597202009 Articular Surface CR ART SURF 12/PURPLE 09 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.