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. 2,510 recalls have been distributed to Wyoming in the last 12 months.
Showing 12861–12880 of 27,462 recalls
Recalled Item: BioEnvelope Recalled by AZIYO BIOLOGICS Due to Possible suture brittleness...
The Issue: Possible suture brittleness or breakage along the Envelope seam before the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CanGaroo Envelopes labeled as the following: 1. CanGaroo Envelope (Large)...
The Issue: Possible suture brittleness or breakage along the Envelope seam before the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500...
The Issue: Incorrect labeling on the products package. The label on the package shows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System Recalled...
The Issue: Potential need for device replacement - Elective Replacement Indicator (ERI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System Recalled...
The Issue: Potential need for device replacement - Elective Replacement Indicator (ERI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product...
The Issue: Mislabeled needle lengths
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Camera Recalled by Intuitive Surgical, Inc. Due to Some cameras...
The Issue: Some cameras were found to have residual soil adhered to the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by...
The Issue: It has been determined that some units of catheters were not tightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the...
The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...
The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing...
The Issue: Interference can occur between the adolescent attachment bolt and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...
The Issue: Discrepancy between the correct expiration dates on the individual pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...
The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...
The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...
The Issue: A patch was released for a critical remote code execution vulnerability in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9646 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.