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. 938 recalls have been distributed to Indiana in the last 12 months.
Showing 48941–48960 of 53,528 recalls
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pharmalucence Kit for the Preparation of Technetium Tc 99m Sestamibi...
The Issue: Presence of Particulate Matter; particulate found in retain samples
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin Recalled by Sandoz Incorporated Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Sandoz Inc is recalling Cefazolin for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fudge Buttercream Frosted Peanut Butter cookies Recalled by Cheryls Due to...
The Issue: Undeclared allergen due to use of incorrect packaging on peanut butter cookies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lightlife Farmer's Market Veggie Burgers Recalled by Conagra Inc Due to The...
The Issue: The product packaging for Lighthouse Farmer's Market Veggie Burgers may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The information regarding the FILM Mode calibration may have been considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to...
The Issue: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Praziquantel 56.8mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trimix Recalled by Lowlite Investments, Inc. D/B/A Olympia Pharmacy Due to...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminocaproic Acid 250 mg/ml Injection Recalled by Lowlite Investments, Inc....
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Idoxuridine 0.1% Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PEN-DEX-CHLOR Injection Recalled by Lowlite Investments, Inc. D/B/A Olympia...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylcobalamin 1 mg/ml / Folic Acid 2.5 mg/ml Injection Recalled by Lowlite...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Cypionate 2 mg/ml Test Cyp 50 mg/ml Injection Recalled by Lowlite...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meloxicam 5 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorpromazine HCL 100 mg/ml Injection Recalled by Lowlite Investments, Inc....
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enrofloxacin 20 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxapram 20 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.