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. 2,558 recalls have been distributed to Mississippi in the last 12 months.
Showing 16801–16820 of 28,172 recalls
Recalled Item: Radio Capitellum Recalled by Howmedica Osteonics Corp. Due to Revision rate...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: radial head implant #4 (Sterile packed). Orthopedic implant for replacement...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recon Stem Implant non-coated Recalled by Howmedica Osteonics Corp....
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp. Due to...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: radial head implant #3 (Sterile packed). Orthopedic implant for replacement...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensicare Green Surgical Glove Recalled by Medline Industries Inc Due to...
The Issue: Possible open seal on top portion of the package. Could cause breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST TERUMOBCT Recalled by Terumo BCT, Inc. Due to Certain lots of the...
The Issue: Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...
The Issue: Cook has identified that the affected lots may contain wire guides that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...
The Issue: Some contact lenses were associated with complaints of a foreign matter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex(R) Percuvance(TM) Percutaneous Surgical System Recalled by Teleflex...
The Issue: Teleflex is recalling these products because the jaws of the tool tip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BC Thrombin Reagent Kit Lot Number 46751 Recalled by Siemens Healthcare...
The Issue: The BC Thrombin Reagent kit lot 46751 (contains Thrombin Reagent lot 517468)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.