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. 1,781 recalls have been distributed to Indiana in the last 12 months.
Showing 49521–49540 of 53,528 recalls
Recalled Item: 8mm Fenestrated Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Maryland Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Precise Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8 mm Monopolar Curved Scissors (a.k.a. Hot Shears) Manufactured and Recalled...
The Issue: Intuitive Surgical has identified a potential for some units of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system...
The Issue: Siemens became aware of an unintended behavior when using the Luminos dRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...
The Issue: Potential for set screw to be come deformed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL) Recalled...
The Issue: Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Market Pantry Recalled by American Importing Co, Inc Due to American...
The Issue: American Importing Co, Inc is recalling Market Pantry Sweet & Salty Mix...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Non-Thickening Powder Recalled by Novartis Consumer Health Due to...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Supplement Recalled by Novartis Consumer Health Due to The...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Plus Heart Health Non-Thickening Powder Recalled by Novartis...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Fiber Supplement Plus Calcium Recalled by Novartis Consumer Health...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.