CooperVision CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with recall — FDA Z-2150-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Complete FDA and NHTSA recall records dated in 2021, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Out of Specification
Misaligned placement of an axis mark can cause the patient to experience blurred vision
if the user forgets to select the trigger input manually while beam gating is prescribed for the patient, the proton irradiation will be delivered without gating. If the beam is not gated…
There is a potential for the Anti-free flow clip of the administration set to be inverted which may cause unintended free flow if the user fails to follow on screen prompt to close the…
Specific PINs of the Vectris SureScan MRI lead kits contain the incorrect lead electrode spacing information printed on the shelf box and the sterile pack labeling.
Specific lot of Organic Steel Cut Oats, may actually contain Organic Beet Sugar
Lack of functioning Temperature Indicating Devices in retorts
Firm discovered that some containers exhibited post-process spoilage during additional inspection and deployment of product at Distribution Center.
Lack of functioning Temperature Indicating Devices in retorts
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Lack of functioning Temperature Indicating Devices in retorts
Lack of functioning Temperature Indicating Devices in retorts
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Lack of functioning Temperature Indicating Devices in retorts
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Potential of pieces of rubber gasket from production equipment in Tortilla Casserole Bowl.
Internal label review found that their labeling did not properly declare milk (sub ingredient of margarine) or as an allergen
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Shake base contains undeclare milk due to wrong outer-label stating product is Smoothie Base.
Lack of functioning Temperature Indicating Devices in retorts
Canadian Food Inspection Agency tested blueberries and found Cyclospora cayetanensis.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.