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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16721–16740 of 28,654 recalls
Recalled Item: Tissu-Trans FILTRON 500 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to Recalled by Dako...
The Issue: To correct the kit's instructions for use as the storage time for gastric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Syringe Fill 360 Recalled by Shippert Medical Technologies Due...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope ( Model 10967666) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 (Model 10165888) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope Power (Model 10967888) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective (Model 10495568) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective 16 (Model 10891666) Recalled by Siemens Medical...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline 0.9 % Sodium Chloride Injection Recalled by Medline Industries Inc...
The Issue: Packaged with an incorrect overwrap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 (10165977) Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Pneumatic Lithotripter Recalled by Cook Inc. Due to The...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Sterilization Cap Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Single Use Probe Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.