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. 927 recalls have been distributed to Kansas in the last 12 months.
Showing 45101–45120 of 50,117 recalls
Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...
The Issue: The affected lots of the product may contain a contaminant of fungus that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...
The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...
The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to Arrow is...
The Issue: Arrow is recalling the product due to a labeling inconsistency. One portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...
The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Actavis...
The Issue: Failed Dissolution Specifications: Dissolution test results at 8 hour...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Belladonna Alkaloids with Phenobarbital Tablets Recalled by West-Ward...
The Issue: Presence of Foreign Substance: black specks comprised of degraded organic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by West-Ward Pharmaceutical Corp. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Chemistry A1c_3 Calibrators Recalled by Siemens Healthcare Diagnostics...
The Issue: Siemens confirmed that the ADVIA¿ Chemistry Systems HbA1c method exhibits a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and...
The Issue: Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Cannulated Humeral Nail Intended to aid in the Recalled by...
The Issue: The packaging incorrectly depicts the Synthes Titanium Cannulated Humeral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H Recalled by Synthes USA HQ,...
The Issue: The possibility exists that 2.4 mm VA-LCP 2 column distal radius plates from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric...
The Issue: Certain lots of Trochanteric Fixation Nail were distributed to the field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergetics 25 gauge Soft Tip Cannula Recalled by Synergetics Inc Due to One...
The Issue: One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Anastaflo Intravascular Shunt Recalled by Edwards...
The Issue: Edwards Lifesciences is recalling certain lots of the Anastaflo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used Recalled by...
The Issue: Complaints were received of inconsistencies in the expiration dates shown on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.