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. 1,903 recalls have been distributed to Delaware in the last 12 months.
Showing 8081–8100 of 48,330 recalls
Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tobramycin Opthalmic Solution USP Recalled by ALEMBIC PHARMACEUTICALS, INC....
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hamilton-MR1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...
The Issue: The outer package labeling and product etch are for a Size 6, however, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton C1/T1/MR1 Recalled by Hamilton Medical, Inc. Due to Degrading...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVU Functional GI Software Recalled by Diversatek Healthcare Due to GI...
The Issue: GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...
The Issue: During rework of components during the manufacturing process, an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The O-arm O2 Imaging System is a mobile x-ray system Recalled by Medtronic...
The Issue: Ground cable installed incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sausage Maker Instacure #1 Recalled by The Sausage Maker, Inc. Due to...
The Issue: Contains Sodium Nitrite recalled for potential metal contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...
The Issue: Sterility of device may be compromised due to breach of the chevron seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT...
The Issue: A complaint was received indicating that a package contained a TRIGEN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT...
The Issue: A complaint was received indicating that a package contained a TRIGEN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to...
The Issue: A bottle of Copaliner Solvent was inadvertently packaged into a box labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...
The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.