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. 1,924 recalls have been distributed to Indiana in the last 12 months.
Showing 27161–27180 of 53,528 recalls
Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziyad Brand Tahini Recalled by Ziyad Brothers Importing, Inc. Due to...
The Issue: Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: My Way (levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POSEIDON Xtreme PLATINUM 4500 Recalled by Shoreside Enterprises Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (Levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Option Systems Antibacterial Foaming Hand Wash with .3% PCMX Recalled by...
The Issue: Microbial contamination of NonSterile Product; FDA analysis returned out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: screamin' hot (capsaicin) Pain Relieving Gel Recalled by Ideaz Llc Due to...
The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: screamin' menthol (menthol) Pain Relieving Gel Recalled by Ideaz Llc Due to...
The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3.2MM X 560MM COCR THD TIP Recalled by Zimmer Biomet, Inc. Due to The firm...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HexaPOD evo RT Couch Top (also known as HexaPOD evo Module) Recalled by...
The Issue: Upon completion of a 6D workflow, the HexaPOD evo Module may be in a tilted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Correction vector...
The Issue: Correction vector confirmation message is lost if access point is changed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoglobulin M is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apolipoprotein A1 is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoglobulin A is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoglobulin G is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apolipoprotein B is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.