State
73,741 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,377 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,604 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer GmbH is recalling specific cannulated drills because an investigation found they may have been manufactured from a different material than defined in specifications.
ITI is recalling 2018-2019 HINO 268 and 338 vehicles because backup camera displays may revert to factory settings, causing reversed images and increasing crash risk.
Roche Diagnostics is recalling 15 units of Cobas infinity software versions 2.0 through 2.5 because quality control alarms may fail to display after a bottle change.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling CBS 7.5 taps because they may be made from the wrong material. The products were distributed to 41 US states.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a different material than specified. The products were distributed to 41 US states.
LGE Coachworks is recalling 2018-2019 Ford and Freightliner vans because back-up camera displays may revert to factory settings, reversing the image and increasing crash risk.
PL Custom is recalling 2017-2019 Type I and III ambulances because backup camera monitors may revert to factory settings, reversing the image and increasing crash risk.
Remel Inc is recalling Thio Med w/Dex, Hem, Vit K media because it may fail performance testing after 106 days. The expiration date is being shortened to 105 days.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications. The products were distributed to 41 US states.
Zimmer GmbH is recalling specific AO orthopedic drills because they may be made from the wrong material. The products were distributed to 39 US states.
Zimmer GmbH is recalling specific 3.5mm screw drills because they may be made from a different material than specified.
Remel Inc is recalling Thio Med culture media because the product may fail performance testing after 106 days. The expiration date is being shortened from 9 months to 105 days.
Cook Inc. is recalling Kwart Retro-Inject Ureteral Stent Sets because the instructions for use did not include a warning for stent knotting.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the specifications.
Zimmer GmbH is recalling Stryker 2.7mm screw drills because they may have been manufactured from a material different from the specifications.
Zimmer GmbH is recalling CBS micro, countersink, cannulated, AO screws (Item Number ST503004541) because they may have been manufactured from a different material than specified.
Septodont Inc. is recalling 240 cartons of Articadent dental cartridges because the printed cartons contained text for both Articadent and Xylocaine, though the cartridges themselves are correctly labeled.
Remel Inc is recalling Thio Med w/o Ind, w/Dex media because it may fail performance testing after 106 days. The expiration date is shortened from 9 months to 105 days.
Remel Inc is recalling 27 units of Thio Med w/o Ind, w/Dex due to potential failure in performance testing after 106 days.
Zimmer GmbH is recalling Stryker 2.7mm screw drills because they may be made from a different material than specified.
Zimmer GmbH is recalling V-TEK Micro-countersink items because they may be made from the wrong material. The products were distributed to 39 US states.
Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a material different from the defined specifications.
Thommen Medical AG is recalling 15 units of dental adapters for handpieces because the coupling may deform, making removal difficult.