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. 2,385 recalls have been distributed to Oklahoma in the last 12 months.
Showing 44641–44660 of 49,976 recalls
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...
The Issue: Defective Container: Stability samples of both products were noted to have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin PF (BSS) 1% Recalled by Avella of Deer Valley, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 1.25 mg/0.05 mL PF Recalled by Avella of Deer Valley, Inc. Due...
The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...
The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....
The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...
The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...
The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.