Recalls affecting Oklahoma
Notices that name Oklahoma in their distribution area, plus every nationwide recall — nationwide recalls reach Oklahoma too.
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Class II · 4 months ago
Keystone Industries DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Nutrisystem, Chocolate Cheesecake, 2 oz packages, Flow Wrapped recall: Undeclared Allergen (Soy)
Undeclared Allergen (Soy)
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Class II · 4 months ago
International Food Products Corporation Dairy House Ingredient Systems Strawberry recall: Potential for Salmonella
Potential for Salmonella
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Class II · 4 months ago
United States Bakery Great Value Hawaiian Roll 4pk recall: Firm observed oily and sticky substance on direct food contact surface
Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
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Class II · 4 months ago
International Food Products Corporation Legacy Tex Dressing Stabilizer Blend recall: Product tested positive for Salmonella
Product tested positive for Salmonella
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Class II · 4 months ago
International Food Products Corporation Dairy House Ingredient Systems Vanilla Dairy recall: Potential for Salmonella
Potential for Salmonella
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Highest risk · 4 months ago
Joolz Aer2 Car Seat Adapters for Strollers recall: Risk of Serious Injury from Fall Hazard
Risk of Serious Injury from Fall Hazard
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Highest risk · 4 months ago
Arizer Solo III portable electronic vaporizers recall: The pajama sets violate the mandatory safety standards for children's
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
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Class II · 4 months ago
INSPIREMD Inc CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/ recall: Stent delivery system may encounter complications during deployment
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
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Class II · 4 months ago
Berlin Heart Gmbh EXCOR Pediatric Ventricular Assist Device System recall: Blood pump inner package expiration date does not match the outer-correct
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
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Class II · 4 months ago
Abbott Medical Merlin" Patient Care System software Merlin" PCS 3650 programmer Model recall: Software malfunction may occur during pacing capture threshold test
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command…
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Class II · 4 months ago
GE Medical Systems, LLC Allia IGS 7 Pulse angiographic X-ray system recall: GE HealthCare has become aware of a potential issue affecting an electrical
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue…
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Class II · 4 months ago
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm recall: The cannulation of the CCS screw is not centered
The cannulation of the CCS screw is not centered.
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Class II · 4 months ago
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. TDC Veloce" recall: An increase in incidence in complaints of a loose outer knife and reports
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
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Class II · 4 months ago
ICU Medical, Inc. Plum Solo Precision IV Pump, 40001-0401 recall: Under certain conditions, the pump may not display a soft limit alert
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming…
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Class II · 4 months ago
Inter-Med Llc Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall: Some units of Aluminum Chloride Gel contain the package insert for Ferric
Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains…
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Class II · 4 months ago
INSPIREMD Inc Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/ recall: Stent delivery system may encounter complications during deployment
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
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Class II · 4 months ago
ICU Medical, Inc. Plum Duo Infusion Pump, 40002-0401 recall: Under certain conditions, the pump may not display a soft limit alert
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming…
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Class II · 4 months ago
INSPIREMD Inc CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/ recall: Stent delivery system may encounter complications during deployment
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
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Class II · 4 months ago
AVID Medical, Inc. Halyard, Eye Bag Pack. Kit Code: UIEB48-01 recall: Inadvertent distribution of sealed pouches that had not undergone validated
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
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Class II · 4 months ago
DT MedTech, LLC Hintermann Series Talar Implant, Left, Size 2 REF 302112 recall: Through customer complaints, the ankle replacement system was found
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right…
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Class II · 4 months ago
Boston Scientific Corporation Orca Single Use Air/Water and Suction Valves recall: Boston Scientific is initiating a medical device removal of Orca Sterile
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated…
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Class II · 4 months ago
Avanos Medical, Inc. Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
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Class II · 4 months ago
Avanos Medical, Inc. Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.