Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,019 recalls have been distributed to Kansas in the last 12 months.
Showing 19441–19460 of 50,117 recalls
Recalled Item: PICC Set- PR-35052-HPHNM Recalled by Arrow International Inc Due to Product...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT CK-02220 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Maximal Barrier Drape ASK-00002-1A Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT AM-05500 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The potential exists for system movement to be permanently blocked by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow SPINAL ANESTHESIA SET ASA-25090-S Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE COMPONENT AN-05505 Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL NEEDLE KIT SL-05500 Recalled by Arrow International Inc Due...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1 Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUP 30MG/ FENT 400MCG/ML INJ in 20 mL syringe Assurance Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Autologous Serum 20% Eye Drops in 3 mL droppers Assurance Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 9MG/ HYDROM 25MG/ SUF 110MCG/ML INJ in 20 mL Recalled by Assurance...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUADMIX FORTE 30MG/4MG/40MCG/400MCG/ML INJ in 1 mL vial Assurance Infusion...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROM 17MG/PRIALT 5MCG/ML INJ in 20 mL syringe Assurance Infusion Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BAC 800MCG/BUP 6.7MG/CLON 600 MCG/FENT 850MCG/MORP 20MG INJ in 20 Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.