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. 2,443 recalls have been distributed to Oklahoma in the last 12 months.
Showing 36461–36480 of 49,976 recalls
Recalled Item: Dexpanthenol Injection Recalled by Downing Labs, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyanocobalamin Buffered Injectable 3mg/mL Recalled by Downing Labs, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chromium Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myelo-Nate CSF Sampling Kit Recalled by Utah Medical Products, Inc Due to...
The Issue: Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit...
The Issue: Possibility that the catheter peel-away component hub tabs may prematurely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...
The Issue: Complaint investigation concluded that although product quality requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Granny Smith green apples Recalled by Del Monte Fresh Produce N.A.,...
The Issue: Apples have the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...
The Issue: It was reported that packaging was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Donnatal (Phenobarbital Recalled by Rx PAK Due to Labeling: Not elsewhere...
The Issue: Labeling: Not elsewhere classified - Product label incorrectly lists...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SMOKED ALBACORE TUNA Recalled by The Garibaldi Cannery, LLC Due to The...
The Issue: The canned smoked Albacore tuna product is recalled because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SILVER SALMON Recalled by The Garibaldi Cannery, LLC Due to The canned...
The Issue: The canned Silver salmon product is recalled because it has the potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ALBACORE TUNA BELLIES Recalled by The Garibaldi Cannery, LLC Due to The...
The Issue: The canned Albacore tuna bellies product is recalled because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.