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 24801–24820 of 53,528 recalls
Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Binding Site Human IgM Kit (for SPAPLUS) Recalled by The Binding Site Group,...
The Issue: Firm is offering advice to customers experiencing challenges when validating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS T2X table Recalled by Deerfield Imaging, Inc. Due to Table may drift...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Stability Specifications: Out-of-Specification results obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antacid Tablets Recalled by L. Perrigo Company Due to Presence of foreign...
The Issue: Presence of foreign substance: Product found to contain metal particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: puriton EYE RELIEF DROPS Recalled by Kadesh International Due to...
The Issue: Non-Sterility: Product manufactured under non-sterile production conditions.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve)...
The Issue: The product was released into commercial distribution while subject to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR Capillary High Flux Dialyzer Single Use Only Recalled by...
The Issue: Potential for external blood leaks from the dialyzer header
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...
The Issue: Cosmetic imperfections on the surface of some lenses.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duncan Hines Signature Confetti Cake cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duncan Hines Classic Butter Golden cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duncan Hines Classic Classic White cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duncan Hines Classic Classic Yellow cake mix 15.25oz. 12 retail Recalled by...
The Issue: positive finding of Salmonella in a retail sample
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Apricot Chai Tea Recalled by Cedar Lake Tea Due to Organic Apricot Chai...
The Issue: Organic Apricot Chai Loose Tea is being recalled due to potential glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...
The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...
The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...
The Issue: The firm has detected a potential risk using the command. After releasing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ascom Telligence Nurse Call System Recalled by Ascom (US) Inc. Due to There...
The Issue: There is an issue that could cause the Telligence System Gateway II, NGGTWY2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.