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. 2,547 recalls have been distributed to Indiana in the last 12 months.
Showing 25381–25400 of 53,528 recalls
Recalled Item: Tri-Mix XL 150 mg/10 mg/100 mcg a) Injectable NDC 69699-1353-10 Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epi-Shugarcaine Kit Solution Pharm D Solutions Recalled by Pharm D...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylcobalamin 1 mg/mL a) 10 mL Injectable NDC 69699-1501-10 Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phosphate Buffer Solution 0.05 m Aqueous Solution Recalled by Pharm D...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin/GHRP-2/Theanine/Mannitol 15 mg/6 mg/75 mg/300 mg Powder Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin E1 150 mcg/mL Injectable Recalled by Pharm D Solutions, LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG Reconstitued 6000 IU Injectable Recalled by Pharm D Solutions, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VISIONIST X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...
The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...
The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME)...
The Issue: Firm identified an issue in the manufacturing process which might contribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...
The Issue: Potential for outer pouch sterile barrier to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO Pacemaker Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APS Accelerator modular systems Recalled by Abbott Laboratories, Inc Due to...
The Issue: The firm identified customer sites where modules which the safety pacemaker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...
The Issue: The action is being initiated because the cooling indicator board was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codan Filter (Codan catalog number BC 693) used with Medrad Recalled by...
The Issue: Bayer has received reports of loose particulate in the filter when the dust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.