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. 2,560 recalls have been distributed to Indiana in the last 12 months.
Showing 24541–24560 of 53,528 recalls
Recalled Item: Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC Recalled...
The Issue: This recall has been initiated due to a change in packaging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...
The Issue: A software update is being issued to correct multiple issues identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...
The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm Recalled by...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J Type Bone Marrow Needle 13ga x 6cm - Product Recalled by Angiotech (Manan...
The Issue: Argon Medical has identified an internal manufacturing issue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.) Recalled...
The Issue: Product was packaged with the Incorrect tamper proof battery door.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...
The Issue: There is a potential for a communication interruption following a bolus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fannie May Pixies Recalled by Fannie May Confections Brands, Inc Due to The...
The Issue: The products outer holiday wrap has an information panel that is incorrect....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Peanut Honey Sea Salt Butter Recalled by Oskri Corp. Due to...
The Issue: Sunflower and Tahini Butter has the potential to be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cashew Coconut Butter Recalled by Oskri Corp. Due to Potential Listeria...
The Issue: Sunflower and Tahini Butter has the potential to be contaminated with...
Recommended Action: Do not consume. Return to store for a refund or discard.