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 29301–29320 of 55,415 recalls
Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...
The Issue: Presence of particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn Inc Due to CGMP Deviations:...
The Issue: CGMP Deviations: Inadvertent release of a drug product with unapproved...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: identified as polyethylene, which is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...
The Issue: Failed Impurities/Degradation Specifications: High out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Luxurious Eye & Lip Collection contains Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermaPro Waterproof Silicone Tape Recalled by Safe N Simple, LLC Due to The...
The Issue: The recalling firm received a customer complaint stating the tape was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vado Steerable Sheath 8.8F Recalled by Kalila Medical Due to Torn sheath...
The Issue: Torn sheath liner material was detected at the proximal end of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent...
The Issue: Falsely elevated results may be obtained when using the ARCHITECT DHEA-S...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 K2 Hemodialysis Machine with software version 5.40 Recalled by...
The Issue: When the recirculation ultrafiltration (UF) Goal is set to a value greater...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vado Bi-Directional Steerable Sheath 8.8F Recalled by Kalila Medical Due to...
The Issue: Torn sheath liner material was detected at the proximal end of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with...
The Issue: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signia" Power Handle (SIGPHANDLE Recalled by Covidien LLC Due to Product...
The Issue: Product reportedly shutting down during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL)...
The Issue: Failed Stability Specifications: Product stability testing results did not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 365 brand Egg Nog Recalled by Harrisburg Dairies, Inc Due to Dried Egg Yolks...
The Issue: Dried Egg Yolks was not specifically stated in ingredient statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rachael's SPRINGFIELD SMOKED FISH STRAWBERRY CREAM CHEESE SPREAD Recalled by...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.