Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,792 recalls have been distributed to Delaware in the last 12 months.
Showing 28441–28460 of 48,330 recalls
Recalled Item: COMP 12MM HUM FRAC STEM MACRO Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER OPTION TYPE 1 TPR SLEVE -6 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM LT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...
The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...
The Issue: Inadequate seal due to lack of adhesive glue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G & W Clobetasol Propionate Ointment 0.05% Recalled by G & W Laboratories,...
The Issue: Failed impurities/degradation specifications: This product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Hyclate USP Recalled by American Pharmaceutical Ingredients LLC...
The Issue: Labeling: Not Elsewhere Classified. Manufacturer and product were discovered...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Option 2 Recalled by L. Perrigo Company Due to Defective Container: Carton...
The Issue: Defective Container: Carton is missing the tablet blister strip and tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules USP Recalled by Lucid...
The Issue: Failed Tablet/Capsules Specifications: pharmacists complaints for bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tissu-Trans Filtron 500 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 250 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.