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. 2,495 recalls have been distributed to Delaware in the last 12 months.
Showing 21321–21340 of 27,373 recalls
Recalled Item: Triglycerides/Glycerol Blanked. In vitro test for the quantitative...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Workflow SLR Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential exists for order transactions from interfaced HIS (Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D2-40 (Lymphatic Marker) Recalled by Biocare Medical, LLC Due to Firm...
The Issue: Firm discovered that incorrect Instructions for Use were shipped with one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Signal Reagent Recalled by ORTHO-CLINICAL...
The Issue: The Immunodiagnostic Products Signal Reagent, Lot 3082 as the reagent packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System (enGen System) Recalled by Ortho-Clinical...
The Issue: Recapper Caps may fall off of, or be knocked from sample tubes placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1265 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1260 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 Diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75....
The Issue: The product failed to meet the internal established statistical test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Avant Garde Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential safety risk of collision of the LINAC gantry with the patient or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device Recalled by...
The Issue: Potential device damage on the strain relief near the hub area, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator....
The Issue: The Astral device allows clinicians to disable all alarms including those...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to under...
The Issue: under certain circumstances the Cios Alpha system may freeze during a procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Blood Agar (TSA w/sheep blood) plate packaged Recalled by Remel Inc...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.