Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,383 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,383 in last 12 months

Showing 2480124820 of 27,462 recalls

Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...

The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Fujinon Inc

Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...

The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...

The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...

The Issue: Synthes became aware that during a procedure using the Matrix Threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Stryker Craniomaxillofacial Division

Recalled Item: Stryker Part Numbers 79-43903 (3cc) Recalled by Stryker Craniomaxillofacial...

The Issue: Stryker received reports of the desiccant bag in the kit leaking silica gel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Cannulated Humeral Nail Intended to aid in the Recalled by...

The Issue: The packaging incorrectly depicts the Synthes Titanium Cannulated Humeral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synergetics Inc

Recalled Item: Synergetics 25 gauge Soft Tip Cannula Recalled by Synergetics Inc Due to One...

The Issue: One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used Recalled by...

The Issue: Complaints were received of inconsistencies in the expiration dates shown on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Getinge Disinfection

Recalled Item: Getinge 46-Series Medical Washer-Disinfectors Recalled by Getinge...

The Issue: Getinge Disinfection AB initiated a voluntary field safety correction for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and...

The Issue: Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric...

The Issue: Certain lots of Trochanteric Fixation Nail were distributed to the field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H Recalled by Synthes USA HQ,...

The Issue: The possibility exists that 2.4 mm VA-LCP 2 column distal radius plates from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended Recalled by...

The Issue: A complaint was reported regarding a screw being found in a package labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Anastaflo Intravascular Shunt Recalled by Edwards...

The Issue: Edwards Lifesciences is recalling certain lots of the Anastaflo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Chemistry A1c_3 Calibrators Recalled by Siemens Healthcare Diagnostics...

The Issue: Siemens confirmed that the ADVIA¿ Chemistry Systems HbA1c method exhibits a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! Multi-Drug Test Panel Product Usage- Labeled as FOR Recalled...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! 1- Panel Test Kit-COC Product Usage- Labeled as Recalled by...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! 1- Panel Test Kit-OPI Product Usage: Labeled as Recalled by...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2013· Sarken, Inc.

Recalled Item: SARKEN STAT! Multi-Drug Test Panel Product Usage- Labeled as FOR Recalled...

The Issue: These products are being recalled because they were distributed without...

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

Class II — Potential Health HazardOngoing