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. 2,566 recalls have been distributed to Kansas in the last 12 months.
Showing 11361–11380 of 28,538 recalls
Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides (ALKP is not affected)...
The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2...
The Issue: Incorrect lot number for Standard Oral Fluid Negative Calibrator on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products TBIL Slides- 5 PACK/300 SLDS In vitro Recalled by...
The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products BuBc Slides - in vitro diagnostic use Recalled by...
The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate...
The Issue: Incorrect lot number for Standard Oral Fluid Negative Calibrator on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are...
The Issue: Potential risk of brush detachment during cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...
The Issue: The plastic housing on the device may fracture
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APPX 0.75ml Recalled by ICU Medical, Inc. Due to Identification of a...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7 IN (18CM) APPX 0.26ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 0.82 ml Recalled by ICU Medical, Inc. Due to Identification of a...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way Recalled by ICU Medical,...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.