Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,547 recalls have been distributed to Louisiana in the last 12 months.
Showing 21221–21240 of 51,202 recalls
Recalled Item: BIOMOD PORCOAT HA GLENTRAY Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Custom Products Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on 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: 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: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...
The Issue: Subpotent Drug: Out of specification result during stability study in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a...
The Issue: FungusAmongUs Shiitake Organic Mushrooms are recalled due to undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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: 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: 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: 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: 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 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: Bubbies Mochi Ice Cream -Chocolate Mint Item Code CS812083 Recalled by...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.