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. 2,642 recalls have been distributed to Oklahoma in the last 12 months.
Showing 7121–7140 of 28,654 recalls
Recalled Item: Lamaze Chill Teether Recalled by Tomy International Inc. Due to Affected...
The Issue: Affected lots of the product are being recalled due to potential microbial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Source Administration Set (SAS) used with the Medrad Intego PET Infusion...
The Issue: Black specks may be present on the packaged needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ActiveAid 922 Recalled by Altimate Medical, Inc. Due to Device manufactured...
The Issue: Device manufactured with a component with affects the foldability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular...
The Issue: Packaging sterile barrier has been compromised. Open seals can lead to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Modular Arthrodesis Nail Recalled by Biomet, Inc. Due to Product missing...
The Issue: Product missing the four small locking collar bolts resulting in extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2¿ - Recalled...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Trak Clavicle Screws Part Number/Part Description: 40-0136 3.0mm x 80mm...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcuTwist Acutrak Compression Screws Part Number/Part Description: AI-0010-S...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid...
The Issue: Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity Reaction Vessels Recalled by Abbott Laboratories Due to Reaction...
The Issue: Reaction vessels may contain a potential contaminant that could affect their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max (VF11) Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 300 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the...
The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic...
The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...
The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use...
The Issue: Concentration of Rheumatoid Factor has decreased in Specific Protein Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.