Complete FDA and NHTSA recall records dated in 2020, 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 missing component (hand suction pump) in the emergency medical kits.
The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
The therapy switch may fail, resulting in the device exhibiting the following behaviors: the device may not perform the selected function, the therapy knob may not change to the energy…
The lidstock states the incorrect expiration date for the product. This issue could result in use of a device that is expired which could potentially lead to an increased risk of infection…
The reported stress crack in the port of the swivel elbow where the flip cap is inserted could result in leakage from the breathing system resulting in the prescribed ventilation not being…
1) 1) Potential intermittent issue may cause image data problems, may lead to artifacts; 2) Potential intermittent scout scanning interruption due to angle signal drift caused by external…
There are potential issues related to the operational state of the scanner, specifically for transport and inadvertent system shutdowns. There could be a possibility of potential delay in…
An instrument failure mode that may result in a Blood Culture Gram Positive (BC-GP) or Gram Negative (BC-GN) false negative call.
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.
The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
High rate of galling of one threaded component.
The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
An instrument failure mode that may result in a Blood Culture Gram Positive (BC-GP) or Gram Negative (BC-GN) false negative call.
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
The firm used pan release spray, which contains soy lecithin, on equipment and finished products labels do not declare soy lecithin.
The firm used pan release spray, which contains soy lecithin, on equipment and finished product label does not declare soy lecithin.
The firm used pan release spray, which contains soy lecithin, on equipment and finished products labels do not declare soy lecithin.
The firm used pan release spray, which contains soy lecithin, on equipment and finished products labels do not declare soy lecithin.
The firm used pan release spray, which contains soy lecithin, on equipment and finished products labels do not declare soy lecithin.
The firm used pan release spray, which contains soy lecithin, on equipment and finished products labels do not declare soy lecithin.
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.
