State

Delaware product recalls

20,371 recalls have nationwide distribution and so reach Delaware. 0 additional recalls listed Delaware specifically in their distribution scope.

About recalls in Delaware

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Delaware consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14976–15000 of 20371

ModerateCPSC·23717·2022-12-15
Crate and Barrel Thornhill Baby Cribs Recalled for Fall Hazard
Crate and Barrel is recalling about 280 Thornhill baby cribs because mattress support pins can become loose or not fit properly, causing the mattress to fall. The firm received six reports of the mattress support pins not fitting correctly or falling out, though no injuries have been reported.
Product
Thornhill Dark Brown and Natural Baby Cribs
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0330-2023·2022-12-14
Sensititre Medical Device Recall: False Antibiotic Susceptibility Test Results
Remel Inc. is recalling Sensititre HPB1 diagnostic plates that may produce false susceptible results for specific bacteria when tested with seven antibiotics. This could lead to inaccurate susceptibility information affecting clinical treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0334-2023·2022-12-14
Sensititre STP6F diagnostic plates may report false antibiotic susceptibility results
Remel's Sensititre STP6F diagnostic plates may produce false susceptible results for Gram-negative bacteria when tested with certain antibiotics, potentially leading to inappropriate treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0338-2023·2022-12-14
FDA Class I Recall: CAIRE Liberator 30 Liquid Oxygen System Units
Caire, Inc. is recalling five CAIRE Liberator 30 liquid oxygen system units due to weld defects on the inner bottle that could lead to device failure and loss of oxygen supply to dependent patients.
Product
CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0328-2023·2022-12-14
Medical Device Recall: Sensititre GN6F May Report False Antibiotic Susceptibility Results
The FDA recalled Sensititre GN6F Gram Negative antimicrobial susceptibility test plates (2,471 units) because they may report false results indicating bacteria are susceptible to certain antibiotics when they are actually resistant.
Product
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0337-2023·2022-12-14
Liquid Oxygen System Devices Recalled Due to Weld Quality Issues
Caire Inc. is recalling 70 CAIRE Liberator 45 liquid oxygen systems due to inconsistencies in weld penetration on the inner bottle's longitudinal weld seam discovered during an audit.
Product
CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0331-2023·2022-12-14
Medical Diagnostic Plate Recalled for False Antibiotic Susceptibility Test Results
Remel Inc is recalling 588 units of the Sensititre Gram Negative IVD AST diagnostic plate due to false susceptible test results for certain bacteria when tested with specific antibiotics. The defect could lead to incorrect treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0332-2023·2022-12-14
FDA Class I Recall: Thermo Sensititre Gram Negative Diagnostic Test Inaccuracy
Thermo Scientific Sensititre CMC7AFLF Gram Negative diagnostic tests may produce false susceptible results for certain bacteria, potentially leading to ineffective antibiotic treatment decisions. The FDA has classified this as a Class I recall.
Product
Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0333-2023·2022-12-14
Gram-negative antibiotic susceptibility test device recalled for false susceptible results
Sensititre MDRGN3F antibiotic test device may return false susceptible results for certain gram-negative bacteria, risking inappropriate antibiotic treatment. FDA Class I recall issued.
Product
Thermo SCIENTIFIC, Sensititre MDRGN3F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0336-2023·2022-12-14
Caire Liberator 45 Liquid Oxygen System Recalled for Weld Defects
Caire, Inc. is recalling 10 CAIRE Liberator 45 liquid oxygen system units due to inconsistencies in weld penetration on the inner bottle discovered during an FDA audit.
Product
CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0329-2023·2022-12-14
Sensititre GN7F Antibiotic Test Plates Recalled for Inaccurate Susceptibility Results
Remel Inc. recalled 8,073 units of Sensititre GN7F antibiotic susceptibility test plates after discovering they may report false results for certain bacteria, potentially leading to incorrect antibiotic treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0339-2023·2022-12-14
CAIRE Liberator 20 Liquid Oxygen System Recalled for Weld Defects
Caire, Inc. is recalling CAIRE Liberator 20 liquid oxygen system units due to weld penetration inconsistencies discovered during an FDA audit. The manufacturing defect affects 3 units.
Product
CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0335-2023·2022-12-14
Medical Device Recall: Sensititre Test Produces False Antibiotic Susceptibility Results
Remel Inc. is recalling a diagnostic test that may incorrectly report antibiotic susceptibility in certain Gram-negative bacteria. False results could lead to inappropriate antibiotic treatment.
Product
Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0327-2023·2022-12-14
Thermo Sensititre diagnostic plate recalled for false susceptibility results
Sensititre diagnostic plates may give false antibiotic susceptibility results for certain bacteria species, potentially affecting treatment decisions. The FDA issued a Class I recall for approximately 1,917 units distributed nationwide.
Product
Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0415-2023·2022-12-14
CareFusion Bipolar Forceps Recalled Due to Incomplete Instructions
CareFusion recalls 142 units of bipolar surgical forceps due to incomplete Instructions for Use lacking power supply interface and maintenance guidance found in the manufacturer's version.
Product
CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.0MM TIP, STR, MED, INSULATED OVERALL LENGTH 8-3/4" (225MM), REF F-5303
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0361-2023·2022-12-14
Dover Urinary Catheter Drainage Bag Port Occlusion Recall
Cardinal Health is recalling Dover closed urethral catheter trays due to potential occlusion of the drainage bag inlet port, which may prevent proper urine drainage and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag Product Code: 3450LF Intended for urinary drainage from the bladder of a patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0397-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar surgical forceps recalled due to incomplete Instructions for Use missing power supply interface and maintenance guidance.
Product
CareFusion V. Mueller euro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0360-2023·2022-12-14
Dover urinary catheter drainage bag occlusion defect nationwide recall
Cardinal Health is recalling Dover urinary catheter trays due to potential blockage of the drainage bag inlet port, which may prevent urine drainage and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag Product Code: 3450 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0373-2023·2022-12-14
Surgical Bipolar Forceps Recalled Due to Missing Operating and Maintenance Instructions
CareFusion is recalling 1369 units of V. Mueller bipolar surgical forceps (Model F-1000) due to incomplete instructions for use. The provided instructions lack information about power supply interface and cleaning and maintenance procedures.
Product
CareFusion V. Mueller CUSHING BAYONET BIPOLAR INSULATED FORCEPS, 0.7MM TIP OVERALL LENGTH 7-1/2" (190MM) , REF F-1000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0405-2023·2022-12-14
Bipolar forceps Instructions for Use missing power supply and maintenance information
CareFusion bipolar forceps have incomplete Instructions for Use missing power supply interface and maintenance guidance. Users should obtain complete instructions from the manufacturer before use.
Product
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5067
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0408-2023·2022-12-14
Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar forceps recalled nationwide due to incomplete Instructions for Use missing power supply interface and cleaning information. The missing content could affect proper device operation and maintenance.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 1.5MM TIP, STRAIGHT STANDARD, 8-3/4" (225MM), REF F-5124
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0075-2023·2022-12-14
Injectable Sodium Chloride Solution Recalled Due to Sterility Concerns and Leakage
Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection due to lack of sterility assurance from potential leakage. The nationwide recall affects injectable saline bags distributed in the United States.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0462-2023·2022-12-14
Philips MR 7700 System Recalled for Gradient Coil Fire Risk
Philips is recalling 566 MR 7700 MRI systems nationwide. The gradient coil in these systems may overheat and produce fire or smoke.
Product
Philips MR 7700 System, Model Number 782120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0358-2023·2022-12-14
Dover Urinary Catheter Drainage Tray Recall Due to Blockage Risk
Cardinal Health is recalling Dover Closed Urethral Tray urinary drainage systems due to potential blockage of the drainage bag inlet port, which may prevent proper bladder emptying and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 14 Fr/Ch (4.7 mm) Product Code: 3410 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0413-2023·2022-12-14
Bipolar Forceps Recall: Incomplete Instructions for Surgical Device
BD recalls CareFusion bipolar forceps (Ref F-5301) due to incomplete Instructions For Use. The IFU is missing information about power supply interface and cleaning and maintenance.
Product
CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.5MM TIP, STRAIGHT, INSULATED OVERALL LENGTH 8-3/4" (225MM), REF F-5301
Category
Medical Device
Distribution
Distributed nationwide