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. 2,553 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,553 in last 12 months

Showing 1750117520 of 28,172 recalls

Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 18"x22" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13.5" Heat Seal Pouch 200 pouches per box Recalled...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x22" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 9"x100'. One roll per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x22" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 4"x8" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3"x8" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Custom Assemblies Inc

Recalled Item: Various custom surgical kits manufactured for CMS Recalled by Custom...

The Issue: The firm manufactured and distributed custom surgical kits which contained...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2017· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: ArjoHuntleigh Flowtron ACS900 Recalled by Arjo, Inc. dba ArjoHuntleigh Due...

The Issue: Reports of the device failure involving delivering continuous pressure to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...

The Issue: Manufacturing process used to assemble the circuit board may result in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...

The Issue: Manufacturing process used to assemble the circuit board may result in some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to BD initiated the...

The Issue: BD initiated the recall of Alaris PC unit model 8015 after the firm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Recalled by Roche...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Invuity, Inc.

Recalled Item: INVUITY(R) PhotonBlade(TM) Recalled by Invuity, Inc. Due to A small number...

The Issue: A small number of customer observations were recently received which related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing