Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,591 recalls have been distributed to Mississippi in the last 12 months.
Showing 14301–14320 of 28,172 recalls
Recalled Item: Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled...
The Issue: Frayed pieces of the mounting card being inside the primary packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medica Wash1-Wash solution used prior to Lipase assay on the Recalled by...
The Issue: Wash1 solution is ineffective in cleaning dispensing probe of TRIG and LDL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ PCV Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Locking Femoral Impactor Recalled by Encore Medical, Lp Due to The...
The Issue: The firm has received reports/complaints concerning the breakage of the tips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plain and Chromic Gut Absorbable Surgical Sutures Recalled by CP Medical Inc...
The Issue: Potential compromise of product sterility after routine monitoring for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US Endoscopy Padlock Clip defect closure system The Recalled by US Endoscopy...
The Issue: Potential esophageal laceration during a patient procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Transseptal Needle Recalled by Cook Inc. Due to The products were...
The Issue: The products were manufactured without a back bevel on the needle tip. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...
The Issue: Potential for the Semi-Rigid canister lid to fragment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use...
The Issue: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velofix SA cervical cage Recalled by U&I CORP. Due to The vertical...
The Issue: The vertical dimensions of screw-hole position in some standalone cages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TASE 400 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...
The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TASE 500 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...
The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.