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. 2,544 recalls have been distributed to Indiana in the last 12 months.
Showing 31281–31300 of 53,528 recalls
Recalled Item: APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 Recalled by Toshiba...
The Issue: When Continuous Trace method is used as the tracing method on Spectral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APLIO 500 TUS-A500 diagnostic ultrasound system Recalled by Toshiba American...
The Issue: When Continuous Trace method is used as the tracing method on Spectral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Needle Recalled by Cook Inc. Due to COOK Medical is...
The Issue: COOK Medical is initiating a voluntary recall of multiple products because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LapSac Introducer Set Recalled by Cook Inc. Due to COOK Medical is...
The Issue: COOK Medical is initiating a voluntary recall of multiple products because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LapSac Introducer Recalled by Cook Inc. Due to COOK Medical is initiating a...
The Issue: COOK Medical is initiating a voluntary recall of multiple products because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protein Bar 14 bars/box Recalled by Herbalife International Of America Inc...
The Issue: Herbalife is recalling Protein Bar-Peanut Butter because it may contain a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic...
The Issue: Failed Impurities/Degradation Specifications: stability testing results did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine HCI Injection Recalled by PAR Sterile Products LLC Due to...
The Issue: Crystallization: due to the presence of white, crystalline particulates,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FEM IM NAIL 14MMDX30CM LEFT Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Transport Monitor/Module Battery Pack Product Usage: intended for...
The Issue: Mindray has received two reports from outside the United States that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Recalled...
The Issue: Potential sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F IM NAIL 10MMDX48CM LG Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 BROAD SCP PLT 26-H STER Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIBIAL I/M NAIL 15MMDX26CM Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II STD TUBE 130DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Offset Stem Extension Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is conducting a lot-specific medical device field action for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM IM NAIL 15MMDX30CM Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...
The Issue: PEG kits have the potential for one of the following defects: missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.