Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

27876–27900 of 50462

HighFDA (Food)·F-1851-2018·2018-08-29
Pacific Coast Fruit Recalls Chopped Spinach Due to Cyclospora Risk
Pacific Coast Fruit Company is recalling 126 cases of chopped spinach in Oregon due to potential Cyclospora contamination.
Product
Spinach Chopped 1", item # 73039. packaged in plastic bag, each case contains 2/5# bags, There are case labels and no unit label. UPC on case label 0 20728 73039. The case label is read in part: "***SPINACH CHOPPED 1" *** 2/5#***73039***PACIFIC COAST FRUIT, PORTLAND, OR…
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2842-2018·2018-08-29
Philips DigitalDiagnost 4 Flex Footplate Recall Due to Injury Risk
Philips is recalling two DigitalDiagnost 4 Flex units because a defective hook allows the footplate to fall, posing an injury risk to patients or operators.
Product
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2861-2018·2018-08-29
Philips DigitalDiagnost Release 3 Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing an injury risk to patients or operators.
Product
DigitalDiagnost Release 3 (Stitching Patient Support) 712025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1833-2018·2018-08-29
Dole Classic Coleslaw Recalled for Potential Metal Fragments
Dole Fresh Vegetables is recalling a limited quantity of Classic Coleslaw due to the potential for metal fragments in the product.
Product
Dole Classic Coleslaw, 14 oz. (397 g) plastic bag; Green Cabbage, shredded carrots. UPC Code 7143001066 Distributed by Dole Fresh Vegetables, Inc., Monterey, CA Case - 10.5 lbs - 12-14 oz. bags. (01) 20071430010666; (10) 2012006212W 8653
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-2850-2018·2018-08-29
Philips DigitalDiagnost 4 Flex Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost 4 Flex and Value units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1836-2018·2018-08-29
Bantam Bagels Recalls Mini Stuffed Bagels Due to Undeclared Egg
Bantam Bagels is recalling 1,452 packages of frozen mini stuffed bagels in California because they contain undeclared egg.
Product
BANTAM BAGELS The Classic Mini Stuffed Bagels PLAIN BAGEL STUFFED WITH PLAIN WHIPPED CREAM CHEESE with large white sticker on the front of the packaging that states EGG TEST 5/04/2018, Frozen
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2897-2018·2018-08-29
Richard Wolf Artholine Punch B 4, 6MM H 1, 6MM Recalled for Potential Injury Risk
Richard Wolf GmbH is recalling 12 units of Artholine Punch B 4, 6MM H 1, 6MM because a potential burr in the joint may increase the risk of injury when the device is opened.
Product
Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created passages. Product Usage: Device is a standard punch; standard punches are used for the removal of soft tissue, cartilage…
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2847-2018·2018-08-29
Philips CombiDiagnost R90 Footplate Hook Recall for Injury Risk
Philips is recalling CombiDiagnost R90 units because a defective hook may allow the footplate to fall, posing an injury risk to patients or operators.
Product
CombiDiagnost R90 (Stitching Patient Support) 709030
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2849-2018·2018-08-29
Philips DigitalDiagnost 4 Chest Footplate Recall Due to Injury Risk
Philips is recalling DigitalDiagnost 4 Chest units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2869-2018·2018-08-29
BD BBL GC-Lect Agar Recalled Due to Incorrect Antibiotic Ingredient
Becton Dickinson is recalling BD BBL GC-Lect Agar plates because some were made with Gentamicin instead of Vancomycin, which may cause false negative gonorrhea test results.
Product
BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of Neisseria gonorrhoeae and better inhibition of contamination bacteria and fungi.
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-2873-2018·2018-08-29
GE Healthcare Optima CT660 Systems Recalled for Damaged Cable Hazard
GE Healthcare is recalling Optima CT660 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Optima CT660. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold only outside the U.S. under the following product names: CT OPTIMA 660, CT OPTIMA 660 LONG BJG SKD RUS, CT OPTIMA 660 LONG BJG SKD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2840-2018·2018-08-29
Elekta Digital Accelerator Recall for Potential Uncontrolled Detector Arm Extension
Elekta is recalling 2,998 Digital Accelerators worldwide due to a potential for uncontrolled extension of iViewGT or XVI detector arms.
Product
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise Digital Accelerator, Infinity, Axesse, and Versa HD
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18763·2018-08-29
BSN Sports Recalls Rubber Critter Toys for Lead Paint Violation
BSN Sports is recalling rubber critter toys because the orange and yellow paint contains lead levels exceeding federal bans. No injuries have been reported.
Product
Rubber critter toys
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1847-2018·2018-08-29
Reser's Fine Foods Recalls Pasta Spinach with Cavatappi Due to Cyclospora Risk
Reser's Fine Foods is recalling specific lots of Pasta Spinach with Cavatappi because the spinach ingredient may be contaminated with Cyclospora.
Product
Pasta Spinach with Cavatappi, Reser's Fine Food, item # 71117.14163, 2/4.5 # packages. UPC 0 71117 14163 4. Product is pasta salads with vinaigrette dressings and vegetables including spinach. All products are in white plastic tubs with labeled lids packed 2/4.5 # to a…
Category
Food
Distribution
13 states
HighFDA (Food)·F-1849-2018·2018-08-29
Reser's Fine Foods Recalls Bow Tie Florentine Pasta Salad Due to Cyclospora Risk
Reser's Fine Foods is recalling Bow Tie Florentine pasta salad because it contains spinach potentially contaminated with Cyclospora. The product is distributed in 12 US states and Canada.
Product
Bow Tie Florentine Reser's Fine Foods, item # 71117.15314, 2/4.5 # packages. UPC 0 71117 15314 9. Product is pasta salads with vinaigrette dressings and vegetables including spinach. All products are in white plastic tubs with labeled lids packed 2/4.5 # to a corrugated…
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-2858-2018·2018-08-29
Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost Dual Detector units because the footplate hook may fail, causing the plate to fall and injure patients or operators.
Product
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2854-2018·2018-08-29
Philips DigitalDiagnost 4.1 Flex Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost 4.1 Flex and Value units because the footplate hook may fail, causing the footplate to fall and injure patients or operators.
Product
DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2870-2018·2018-08-29
GE Healthcare Recalls CT Systems Due to Damaged Cable Electrical Hazard
GE Healthcare is recalling specific CT systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold under the following product names: CT GOLDSEAL LIGHTSPEED ULTRA, CT OPTIMA 660, CT OPTIMA…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2839-2018·2018-08-29
Hitachi Scenaria CT System Recalled for Table Motion Hazard
Hitachi is recalling one Scenaria CT system in Texas because the patient table failed to stop and contacted the gantry, posing a risk of injury.
Product
Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and vascular X-ray Computed Tomography applications in patients of all ages. The images can be acquired in either axial, helical, gated or dynamic modes. The volume…
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2864-2018·2018-08-29
Philips DigitalDiagnost Upgrades Recalled Due to Footplate Safety Hazard
Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Upgrades (Stitching Patient Support) 712083
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2834-2018·2018-08-29
Liebel-Flarsheim Direct Digital Imaging System Recalled for Software Display Discrepancy
Liebel-Flarsheim is recalling 28 Direct Digital Imaging Systems due to a software issue causing significant discrepancies between display and dosimeter readings in pediatric modes.
Product
Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures requiring a beam of diagnostic quality radiation, primarily for urological applications such as functional x-ray diagnostics…
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-2853-2018·2018-08-29
Philips DigitalDiagnost 4.1 Chest X-Ray Unit Recalled for Footplate Hazard
Philips is recalling DigitalDiagnost 4.1 Chest X-Ray units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2868-2018·2018-08-29
Philips EasyDiagnost Eleva DRF Footplate Hook Recall
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2859-2018·2018-08-29
Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost Dual Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2867-2018·2018-08-29
Philips EasyDiagnost Eleva DRF Footplate Recall for Injury Risk
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
EasyDiagnost Eleva DRF (Stitching Patient Support) 706032
Category
Medical Device
Distribution
Distributed nationwide