The Recall Desk

State

Alabama product recalls

73,817 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,378
Critical
1,129
Severe
1,605
Most recent
2026-11-04

Of the 6,378 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 1,605 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47376–47400 of 80195

  • SevereFDA (Devices)·Z-2068-2017·2017-05-17

    Zimmer Biomet Recalls Regenerex Patella Implants Due to Peg Shearing

    Zimmer Biomet is recalling 8,154 Regenerex Series A Patella implants because the pegs may shear after surgery.

    Product
    Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product Usage: The Regenerex Series A Patella can be used for any non-cemented resurfaced 3-peg patella application within the Vanguard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2203-2017·2017-05-17

    Reser's Macaroni Salad Recalled for Undeclared Milk and Soy Allergens

    Reser's Fine Foods is recalling American Classics Macaroni Salad because it contains undeclared milk and soy. The product was distributed to wholesalers in 12 states.

    Product
    Reser's Fine Foods, American Classics Macaroni Salad, Net Wt 1 lb. (454 g) UPC 7117.19007, packaged in 16 oz plastic tubs, 12 per case. Reser's Fine Foods, Inc. Beaverton, OR 97006.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-2212-2017·2017-05-17

    Frito-Lay Recalls Lays Kettle Cooked Multipacks Due to Salmonella Risk

    Frito-Lay is recalling 12-count Lays Kettle Cooked Multipacks nationwide due to potential Salmonella presence.

    Product
    12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2049-2017·2017-05-17

    Roche Diagnostics Recalls Sample Probes for Corrosion-Related Liquid Level Detection Issues

    Roche Diagnostics is recalling 3,946 sample probes for cobas analyzers because corrosion on electrical contacts can disrupt liquid level detection, potentially causing sample carryover.

    Product
    Sample probes associated with: cobas 6000 Series System, cobas 8000 Modular Analyzer Series, cobas c 311 analyzer cobas c 501/502 cobas c 701/702 cobas 8000 ISE Product Usage: The cobas 6000 series is a fully automated, random-access, software-controlled system for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0705-2017·2017-05-17

    Teva Recalls Clozapine Tablets Due to Microbial Contamination

    Teva Pharmaceuticals is recalling specific lots of Clozapine Tablets USP, 25 mg, due to microbial contamination of non-sterile products.

    Product
    Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose Blisters per carton (NDC 0093-4359-93), Individual Blister Pack (NDC 0093-4359-19), Rx Only, Manufactured By: Teva Pharmaceutical Industries Ltd., Jerusalem…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2200-2017·2017-05-17

    Pinnacle Foods Recalls Great Value Bread and Butter Chips for Glass Fragments

    Pinnacle Foods is recalling Great Value Bread and Butter Chips because glass fragments were found in the product. The chips were distributed nationwide.

    Product
    Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716 UPC 078742145990
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2046-2017·2017-05-17

    Arthrex Recalls Anthrex SpeedBridge Implant System Due to Broken Eyelets

    Arthrex, Inc. is recalling the Anthrex SpeedBridge Implant System because some eyelets broke from the SwiveLock Anchor during insertion.

    Product
    Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-2207-2017·2017-05-17

    Treehouse Foods Recalls Macaroni and Cheese Cups for Salmonella Risk

    Treehouse Foods is recalling specific brands of microwaveable macaroni and cheese cups because they may be contaminated with Salmonella.

    Product
    Macaroni & Cheese microwaveable cups sold under the following brands: 1. Big Win Original Macaroni & Cheese Dinner, UPC 11822-58403. 2. Cheese Club express mac Macaroni Cheese Dinner, UPC 41498-17167, 3. Great Value Macaroni & Cheese Dinner, UPC 78742-08249.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V325000·2017-05-17

    Bison Horse Trailers Recalled for Incorrect Weight Rating Labels

    Bison Coach is recalling 2016-2018 horse trailers due to incorrect Gross Axle Weight Rating labels, which may lead to overloading and increased crash risk.

    Product
    BISON — BISON LAREDO, TRAIL HAND, TRAIL BOSS, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17154·2017-05-17

    Cabrinha Recalls Kiteboard Control Systems Due to Injury and Fall Hazards

    Cabrinha is recalling about 2,900 kiteboard control systems because a stainless steel component can break, causing loss of kite control and posing injury and fall hazards.

    Product
    Cabrinha Kiteboard control systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2017·2017-05-17

    Arthrex Bio-SwiveLock SP Vented Anchor Recall Due to Broken Eyelets

    Arthrex, Inc. is recalling specific Bio-SwiveLock SP Vented anchors because some eyelets broke during insertion.

    Product
    Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Devices)·Z-2043-2017·2017-05-17

    Arthrex Bio Composite SwiveLock Anchor Eyelets Break on Insertion

    Arthrex is recalling specific batches of Bio Composite SwiveLock anchors because some eyelets broke during insertion.

    Product
    Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-2040-2017·2017-05-17

    Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Patient ID Error

    Siemens is recalling 159 RAPIDPoint 500 Blood Gas Analyzers because a blank patient ID field may cause demographic errors.

    Product
    RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total hemoglobin, and hemoglobin derivatives in arterial, venous, and capillary whole blood samples.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2054-2017·2017-05-17

    CooperSurgical lnflatoball Pessary Recalled for Incorrect Latex-Free Labeling

    CooperSurgical is recalling lnflatoball Latex Rubber Pessaries because the secondary packaging incorrectly states the product is latex-free, despite being made of 100% latex.

    Product
    CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary Kit. Product Usage: The lnflatoball Pessary is a single-patient use pessary manufactured from natural latex rubber and is used for treating cystocele and/or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2057-2017·2017-05-17

    Med-Hot Thermal Imaging System Recalled for Lack of FDA Clearance

    Med-Hot Thermal Imaging, Inc. is recalling 12 units of the MTI 2000 Thermal Imaging System because the indications for use are not cleared or approved for the U.S. market.

    Product
    MEDHOT MTI 2000 THERMAL IMAGING SYSTEM - TotalVision software with Elevated Body Temperature Screening module, for use as a medical diagnostic purposes as part of a telethermographic system utilizing FLIR cameras, Models A615sc and A315sc. Cameras are private labeled as MAX…
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2071-2017·2017-05-17

    Stryker PROFESS Registration Kit Recalled for Expiration Date Issues

    Stryker is recalling 65 PROFESS Registration Kits shipped near or past their expiration dates. The kits are used for intranasal and sinus surgery.

    Product
    Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2208-2017·2017-05-17

    Vertical Pharmaceuticals Recalls OB Complete Prenatal Multivitamin Due to Labeling Error

    Vertical Pharmaceuticals is recalling one lot of OB Complete with DHA Prenatal Multivitamin because the label claim for Omega-3 Fatty Acids does not match the actual formulation.

    Product
    Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical Pharmaceuticals, LLC Sayreville, NJ 08872 UPC 368025049603
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Drugs)·D-0700-2017·2017-05-17

    Sun Pharmaceutical Recalls Olanzapine Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 7.5 mg, because they failed impurity specifications. The recall covers 6,138 bottles distributed nationwide and in Puerto Rico.

    Product
    Olanzapine Tablets, 7.5 mg, packaged in a) 30-count bottles (NDC 62756-553-83), b) 100-count bottles (NDC 62756-553-88), and c) 1000-count bottles (NDC 62756-553-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0699-2017·2017-05-17

    Sun Pharmaceutical Recalls Olanzapine Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling specific lots of Olanzapine Tablets, 2.5 mg, because they failed impurity specifications.

    Product
    Olanzapine Tablets, 2.5 mg, 1000-count bottles, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-551-18.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2069-2017·2017-05-17

    Almore Microfil Composite Instruments Recalled for Incorrect Sterile Labeling

    Almore International Inc. is recalling Microfil Composite Instruments because packaging labels incorrectly display a sterile symbol, although the devices are not sterile.

    Product
    Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box. Microfil Composite Instruments are intended to be sterilized by the dentist prior to each use. It is used for composite restoration development. The thin…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0702-2017·2017-05-17

    Sun Pharmaceutical Recalls Olanzapine Tablets Due to Impurity Failures

    Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 20 mg, because they failed impurity specifications. The recall covers 14,784 bottles distributed nationwide and in Puerto Rico.

    Product
    Olanzapine Tablets, 20 mg, packaged in a) 30-count bottles (NDC 62756-556-83), b) 100-count bottles (NDC 62756-556-88), and c) 1000-count bottles (NDC 62756-556-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun…
    Category
    Drug
    Distribution
    Distributed nationwide