HIGH
FDA DEVICE
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
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HIGH
FDA DRUG
Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by: Safecor, Columbus, OH 43204. NDC: 64380-474-01
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
ATOMOXETINE
Labeling: Label
HIGH
FDA DEVICE
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067,...
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
It was
HIGH
FDA DEVICE
Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura...
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
It was
HIGH
FDA FOOD
Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g UPC 6 224011 088244 Produced by: AL-MALAZ COMPANY FOR TRADE AND INDUSTRY Piece No. 110-250 acres area Badr City - Egypt
Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.
Nassar Investment Company
Salmonella. The
HIGH
FDA DEVICE
Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number: CI-1601-04 Software Version: N/A Product Description: The HiResolution Bionic...
Due to incorrect shelf-life expiration date.
Advanced Bionics
Due to
HIGH
FDA DEVICE
BD Pyxis MedStation ES REF: 323 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303
Fingerprint scanner
HIGH
FDA DEVICE
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Halyard, Pain Pack. Kit Code: AMPK48-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
AVID Medical
Inadvertent distribution
HIGH
FDA DEVICE
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride
HIGH
FDA DEVICE
Halyard, Drape Pack. Kit Code: LMDP36-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
AVID Medical
Inadvertent distribution
HIGH
FDA DEVICE
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical
Lidocaine hydrochloride