Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,458 recalls have been distributed to Oklahoma in the last 12 months.
Showing 34441–34460 of 49,976 recalls
Recalled Item: Ultrasound Gastroscope Product Usage: Intended to provide optical...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Slide Battery/line powered hydraulic table with removable leg section...
The Issue: The potential exists within the identified tables that incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signmoidoscope Product Usage: Intended to provide optical visualization of...
The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...
The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The Recalled...
The Issue: Empirical Labs is recalling Liposomal Magnesium because of the potential for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cisatracurium Besylate Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Incorrect/ Undeclared Excipient: Firm is recalling product due to an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril & Hydrochlorothiazide Tables Recalled by Lupin Pharmaceuticals...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merge Eye Care Systems Recalled by Merge Healthcare, Inc. Due to The system...
The Issue: The system will completely stop allowing the downloading or acquisition of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare....
The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: When taking measurements from images on the Cardio workstation or from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...
The Issue: An error message can occur resulting in the prior studies being unavailable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software using EchoIMS. The firm name on the Recalled by Merge...
The Issue: A situation can occur allowing two physicians to access the same study...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MasimoSET LNOP DCIP pediatric/slender digit SpO2 reusable sensor Recalled by...
The Issue: Under certain conditions, the cables used with the Hemo system during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MasimoSET LNOP DCI adult SpO2 reusable sensor Recalled by Merge Healthcare,...
The Issue: Under certain conditions, the cables used with the Hemo system during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive when used with RadSuite. The firm name Recalled...
The Issue: The software produced a number of "do not route" exceptions, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive (ICEA) software. iConnect Enterprise Archive is...
The Issue: The study is archived but cannot be opened in iConnect Access and cannot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...
The Issue: The versions allow images to be stored without pixel data, resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Recalled by Merge Healthcare, Inc. Due to Cardio...
The Issue: Cardio study list does not show STAT studies without .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.