Philips Medical Systems (Cleveland) Ingenuity TF PET/CT (non-RoHS), Model Number 882456 This recall — FDA Z-0823-2019
A software update is being issued to correct multiple issues identified in the previous software version.
Complete FDA and NHTSA recall records dated in 2019, 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.
A software update is being issued to correct multiple issues identified in the previous software version.
There is a potential that Wedge IDs were not included in the DICOM RT PLAN sent from the TPS, which will cause the field in MOSAIQ to be created with no wedge. Treatment of a field without…
Evidence supports that when customers performed a fuse replacement as part of a March 2017 field action, the fuse clips became stretched and were no longer mechanically tight with the fuse,…
Some of the installed valve-inserts have a diameter smaller than the specification.
A subset of Medtronic dual chamber pacemakers distributed worldwide between 10 March 2017 and 7 January 2019 under the brand names Adapta, Versa, and Sensia when programmed to a dual…
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
Recalled products were manufactured with an ingredient that is potentially contaminated with Salmonella.
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
The 1.25 oz Forest Wild Wolf Dark Chocolate bars are recalled due to undeclared milk
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
Recalled products were manufactured with an ingredient that is potentially contaminated with Salmonella.
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to…
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
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.