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. 2,469 recalls have been distributed to Delaware in the last 12 months.
Showing 25081–25100 of 27,373 recalls
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO-MED ORTHO TOTAL JOINT TRACECART(R) Recalled by DeRoyal Industries Inc...
The Issue: DeRoyal recalled kits that contained Stryker togas which were recalled for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******QTY 1***APEX Arthroscopy Tubing Set. Intended for use for Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Glidesheath (tm) Recalled by Terumo Medical Corporation Due to...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...
The Issue: When the bed is put into the chair egress position, the magnets on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large Recalled by...
The Issue: Stryker has received reports from customers indicating post-operative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens MEVATRON series Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The information regarding the FILM Mode calibration may have been considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 IR Excimer System (STAR S4 IR) Mfg by AMO Manufacturing USA Recalled...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR VACCESS¿ PTA Balloon Dilatation Catheters Recalled...
The Issue: Bard Peripheral Vascular (BPV) has confirmed that some product code/lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...
The Issue: Product labeled with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S3 ActiveTrack Excimer System (STAR S3) Mfg by AMO Manufacturing USA...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Recalled by...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...
The Issue: DJO, LLC has recently identified a product safety issue with the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.