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. 2,448 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,448 in last 12 months

Showing 2806128080 of 28,172 recalls

Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Staight Microsurgical Needle 3cm...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle 2.75"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle 4.0"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Needle 6.5"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade 6.5...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2010· App Pharmaceuticals Llc

Recalled Item: HEPARIN LOCK FLUSH SOLUTION Recalled by App Pharmaceuticals Llc Due to CGMP...

The Issue: CGMP Deviations: Incomplete documentation associated with test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2010· App Pharmaceuticals Llc

Recalled Item: HEPARIN LOCK FLUSH SOLUTION Recalled by App Pharmaceuticals Llc Due to CGMP...

The Issue: CGMP Deviations: Incomplete documentation associated with test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2010· Cayenne Medical Inc.

Recalled Item: AperFix Femoral Implant Coring Removal Drill Recalled by Cayenne Medical...

The Issue: A review of product complaints in 2010 identified a trend for the Coring...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2010· GE OEC Medical Systems, Inc

Recalled Item: GE HC OEC 9900 Elite and GE OEC 9800 Fluoroscopes Recalled by GE OEC Medical...

The Issue: GE OEC recalled certain 9800 Fluoroscope & 9900 Elite Models because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2010· Philips Healthcare Inc.

Recalled Item: Philips Healthcare Computed Tomography X-Ray System. These devices are...

The Issue: Philips Healthcare discovered the customer was performing CTDI measurements...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2010· Steris Corporation

Recalled Item: A mobile Recalled by Steris Corporation Due to Customers may be storing...

The Issue: Customers may be storing objects on the base and/or around the column of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2010· Mallinckrodt Inc

Recalled Item: The Handi-Fil Disposable Syringe Fill Tube is a sterile plastic tube...

The Issue: A report was received from a Japanese distributor regarding a complaint from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2010· Orthohelix Surgical Designs Inc

Recalled Item: OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT:...

The Issue: The tips of the drivers are breaking while being used to drive the screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2010· Orthohelix Surgical Designs Inc

Recalled Item: OrthoHelix Part #HCS-056-32 3.8MM Cannulated Hex Driver NON STERILE MAT:...

The Issue: The tips of the drivers are breaking while being used to drive the screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2010· Lockheed Martin Gyrocam Systems, Inc.

Recalled Item: Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Recalled by...

The Issue: These camera systems were manufactured by LMGS and found to fail to comply...

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

Class II — Potential Health HazardOngoing