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. 2,655 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,655 in last 12 months

Showing 70817100 of 48,330 recalls

Medical DeviceDecember 1, 2023· Olympus Corporation of the Americas

Recalled Item: SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S Recalled by...

The Issue: Olympus identified inconsistencies in the Instructions for Use regarding...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508...

The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

Recalled Item: Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for Recalled by...

The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

Recalled Item: DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product...

The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· B-K Medical A/S

Recalled Item: bkActiv Ultrasound System 2300 Recalled by B-K Medical A/S Due to An issue...

The Issue: An issue on the Dual Live Compare feature on the bkActiv system could result...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Link Patella Glide Resection Guide- For the implantation of the Recalled by...

The Issue: Mislabeled: Angle and height of the device marked as L(large) corresponds to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Xcision Medical Systems, LLC

Recalled Item: GammaPod - Treatment Planning System-a component of the GammaPod Irradiation...

The Issue: Wrong structures imported into the GammaPod Treatment Planning...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Philips North America Llc

Recalled Item: Spectral CT 7500 Recalled by Philips North America Llc Due to Multiple...

The Issue: Multiple software issues that affect device functionality.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Philips North America

Recalled Item: BrightView X Recalled by Philips North America Due to While using...

The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Philips North America

Recalled Item: BrightView Recalled by Philips North America Due to While using...

The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Philips North America

Recalled Item: BrightView XCT Recalled by Philips North America Due to While using...

The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Boston Scientific Corporation

Recalled Item: Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM)...

The Issue: The software application on the Programmer/Recorder/Monitor (PRM) for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Insulet Corporation

Recalled Item: Omnipod 5 App (on compatible Android smartphones) Recalled by Insulet...

The Issue: The bolus calculator is not recording the decimal point if it is the first...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 30, 2023· Busse Hospital Disposables, Inc.

Recalled Item: Catalog No. 9251R1 Recalled by Busse Hospital Disposables, Inc. Due to Firm...

The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 30, 2023· Busse Hospital Disposables, Inc.

Recalled Item: Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE Recalled by...

The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 30, 2023· Busse Hospital Disposables, Inc.

Recalled Item: Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE Recalled by...

The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
FoodNovember 29, 2023· TGD Cuts, LLC

Recalled Item: MELON LOUPE/DEW CHUNKS 50/2 OZ. Packaged in film. Recalled by TGD Cuts, LLC...

The Issue: Potential Salmonella Contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 29, 2023· TGD Cuts, LLC

Recalled Item: MIXED FRUIT CUBE 1/2"-NO GRA 20 LBS. Packaged in buckets. Recalled by TGD...

The Issue: Potential Salmonella Contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 29, 2023· TGD Cuts, LLC

Recalled Item: MIX FRUIT ALOHA BOWL 3/48 OZ Packaged in clamshell container. Recalled by...

The Issue: Potential Salmonella Contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 29, 2023· TGD Cuts, LLC

Recalled Item: MIXED FRUIT BURST 6/10 OZ Packaged in clamshell containers. Recalled by TGD...

The Issue: Potential Salmonella Contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund