Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,580 recalls have been distributed to Ohio in the last 12 months.
Showing 29561–29580 of 55,415 recalls
Recalled Item: Methylene Blue (PF) 10 mg/mL (1%) Injectable Vial Recalled by KRS Global...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin Acetate 3 mg/ GHRP6 3 mg Recalled by KRS Global Biotechnology,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroquinone 8%/ Tretinoin 0.1% Topical Ointment packaged in jars Recalled...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUADMIX #18 Recalled by KRS Global Biotechnology, Inc Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone 3% Topical Cream packaged in jars Recalled by KRS Global...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol 0.1% (1 mg/gm) Cream packaged in jars Recalled by KRS Global...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 Units in 0.9% Sodium Chloride Solution (PF) IV Bag Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bi-Est (Estriol/Estradiol) (80/20) + Progesterone 7.5 mg/200 mg Cream...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclopentolate HCl/ Phenylephrine HCl/ Tropicamide/ Ketorolac 1%/ 10%/ 1%/...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin 2 Recalled by KRS Global Biotechnology, Inc Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chloramphenicol 500 mg Sulfamethoxazole 500 mg Amphotericin 50 mg Otic...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Roasted & Salted Cashews and Chocolate Covered Cashews Recalled by Meijer...
The Issue: Packages are mislabeled and actually contain undeclared mixed nuts instead...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) Spectra...
The Issue: The Spectra System/Legacy Guided Surgery Handle Kit had guided handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated...
The Issue: Potential for cracked luer hubs
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen CVC Kit Recalled by Arrow International Inc...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.